{
  "@context": {
    "schema": "https://schema.org/",
    "au": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native#",
    "@vocab": "https://schema.org/",
    "claims": {
      "@id": "au:claims",
      "@container": "@list"
    },
    "epistemicStatus": "au:epistemicStatus",
    "occurred": "au:occurred",
    "supported": "au:supported",
    "adjudged": "au:adjudged",
    "operative": "au:operative",
    "grounding": "au:grounding",
    "groundingType": "au:groundingType",
    "adjudicator": "au:adjudicator",
    "source": "au:source",
    "sourceUrl": "au:sourceUrl",
    "value": "au:value",
    "claimType": "au:claimType",
    "reviewStatus": "au:reviewStatus",
    "commercialInfluence": "au:commercialInfluence",
    "falsifier": "au:falsifier"
  },
  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2159-2023.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tANGIOGRAPHY DRP PK PEDI CATH, Model Number 00-401318M;   b)\tANGIOGRAPHY OR, Model Number CDS984944C;   c)\tANGIOGRAM, Model Number DYNJ0149444M;   d)\tEP LAB DEVICE PACK-LF, Model Number DYNJ0160556D;   e)\tVASCULAR ANGIO PACK-LF, Model Number DYNJ0201109AG;   f)\tANGIO PACK-LF, Model Number DYNJ0373279M;   g)\tVISCERAL ANGIOGRAM PACK-LF, Model Number DYNJ0429121I;   h)\tIPMC ANGIOGRAPHY PACK-LF, Model Number DYNJ0806254D;  i)\tANGIOGRAPHY PACK-LF, Model Number DYNJ0854485T;   j)\tANGIO DRAPE PACK, Model Number DYNJ17624B;   k)\tDEPAUL ANGIO PACK, Model Number DYNJ19939M;   l)\tEP ANGIOGRAPHY PACK, Model Number DYNJ24225K;   m)\tANGIOGRAPHY DRAPE PACK-LF, Model Number\tDYNJ28067G;   n)\tDASHTI-YAO NEURO ANGIO-LF, Model Number DYNJ33457C;   o)\tANGIOGRAM TRAY, Model Number DYNJ33638K;   p)\tANGIO PACK, Model Number DYNJ34361;   q)\tANGIO/PICC PACK, Model Number DYNJ36049;   r)\tIR MINOR ANGIO PACK, Model Number\tDYNJ37665B;   s)\tANGIO LEFT HEART PACK, Model Number DYNJ40632C;   t)\tMV-IR ANGIO DRAPE PACK-LF, Model Number DYNJ41553D;   u)\tCUSTOM ANGIO TRAY, Model Number DYNJ41649F;   v)\tFS ANGIO, Model Number DYNJ42499C;   w)\tANGIO PACK, Model Number DYNJ42903B;   x)\tANGIO PACK, Model Number DYNJ43661B;   y)\tANGIOGRAPHY PACK, Model Number DYNJ44293D;   z)\tANGIO DRAPE PACK, Model Number DYNJ44320F;   aa)\tANGIOGRAM PACK, Model Number DYNJ45007;   bb)\tANGIO BASIN SET, Model Number DYNJ46043F;   cc)\tANGIO TRAY, Model Number DYNJ46153B;   dd)\tANGIOGRAM PACK, Model Number DYNJ47004C;   ee)\tANGIO PACK, Model Number DYNJ47226A;   ff)\tANGIOGRAPHY PACK, Model Number DYNJ47906;   gg)\tANGIO DRAPE SPEC PROC PACK-LF, Model Number DYNJ47951A;   hh)\tMH HOOD CARDIAC ANGIO, Model Number DYNJ49884F;   ii)\tANGIO PACK, Model Number DYNJ50624A;   jj)\tANGIO PACK, Model Number DYNJ51239A;  kk)\tANGIO TRAY, Model Number DYNJ52121;   ll)\tANGIO PACK-LF, Model Number DYNJ52898C;   mm)\tANGIOGRAPHY PACK, Model Number DYNJ55252B;   nn)\tANGIOGRAPHY PACK, Model Number DYNJ57498;   oo)\tPERCUTANEOUS ANGIO PACK-LF, Model Number DYNJ57645B;   pp)\tGENERAL ANGIO PACK, Model Number DYNJ57760B;   qq)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792A;   rr)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792B;   ss)\tANGIO PACK, Model Number DYNJ58126A;   tt)\tHH ANGIO PACK, Model Number DYNJ59465B;   uu)\tOR ANGIO PACK, Model Number DYNJ60319A;   vv)\tANGIO PACK 2-A, Model Number DYNJ60507A;   ww)\tFEMORAL ANGIOGRAPY SET UP, Model Number DYNJ61015B;   xx)\tANGIO PACK, Model Number DYNJ62299;   yy)\tCLOVIS CATH LAB PACK, Model Number DYNJ62379;   zz)\tANGIO PACK, Model Number DYNJ62544;   aaa)\tANGIO TRAY W/CHLORAPREP, Model Number DYNJ62742;   bbb)\tOR ANGIO PAC\t, Model Number DYNJ63976A;   ccc)\tSUNSHINE PAC\t, Model Number DYNJ64830;   ddd)\tANGIO PAC\t, Model Number DYNJ65043A;   eee)\tCATH LAB PAC\t, Model Number DYNJ65185;   fff)\tANGIOGRAPHY PACK, Model Number DYNJ65190C;   ggg)\tPACK,BASIC ANGIO, Model Number DYNJ65482A;   hhh)\tANGIO PACK, Model Number DYNJ66398B;   iii)\tANGIOGRAPHY PACK, Model Number DYNJ66476;   jjj)\tSURGERY ANGIO PACK-LF, Model Number DYNJ66500;   kkk)\tOR ANGIOGRAPHY PACK, Model Number DYNJ67245;   lll)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJ68065A;   mmm)\tANGIO TRAY, Model Number DYNJ68758;   nnn)\tANGIO, Model Number\tDYNJ902507B;   ooo)\tANGIOGRAPHY PACK, Model Number DYNJC2371G;   ppp)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJT2344B;   qqq)\tPEDI ANGIO PACK-LF, Model Number PHS41743D",
  "description": "FDA recall Z-2159-2023 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tANGIOGRAPHY DRP PK PEDI CATH, Model Number 00-401318M;   b)\tANGIOGRAPHY OR, Model Number CDS984944C;   c)\tANGIOGRAM, Model Number DYNJ0149444M;   d)\tEP LAB DEVICE PACK-LF, Model Number DYNJ0160556D;   e)\tVASCULAR ANGIO PACK-LF, Model Number DYNJ0201109AG;   f)\tANGIO PACK-LF, Model Number DYNJ0373279M;   g)\tVISCERAL ANGIOGRAM PACK-LF, Model Number DYNJ0429121I;   h)\tIPMC ANGIOGRAPHY PACK-LF, Model Number DYNJ0806254D;  i)\tANGIOGRAPHY PACK-LF, Model Number DYNJ0854485T;   j)\tANGIO DRAPE PACK, Model Number DYNJ17624B;   k)\tDEPAUL ANGIO PACK, Model Number DYNJ19939M;   l)\tEP ANGIOGRAPHY PACK, Model Number DYNJ24225K;   m)\tANGIOGRAPHY DRAPE PACK-LF, Model Number\tDYNJ28067G;   n)\tDASHTI-YAO NEURO ANGIO-LF, Model Number DYNJ33457C;   o)\tANGIOGRAM TRAY, Model Number DYNJ33638K;   p)\tANGIO PACK, Model Number DYNJ34361;   q)\tANGIO/PICC PACK, Model Number DYNJ36049;   r)\tIR MINOR ANGIO PACK, Model Number\tDYNJ37665B;   s)\tANGIO LEFT HEART PACK, Model Number DYNJ40632C;   t)\tMV-IR ANGIO DRAPE PACK-LF, Model Number DYNJ41553D;   u)\tCUSTOM ANGIO TRAY, Model Number DYNJ41649F;   v)\tFS ANGIO, Model Number DYNJ42499C;   w)\tANGIO PACK, Model Number DYNJ42903B;   x)\tANGIO PACK, Model Number DYNJ43661B;   y)\tANGIOGRAPHY PACK, Model Number DYNJ44293D;   z)\tANGIO DRAPE PACK, Model Number DYNJ44320F;   aa)\tANGIOGRAM PACK, Model Number DYNJ45007;   bb)\tANGIO BASIN SET, Model Number DYNJ46043F;   cc)\tANGIO TRAY, Model Number DYNJ46153B;   dd)\tANGIOGRAM PACK, Model Number DYNJ47004C;   ee)\tANGIO PACK, Model Number DYNJ47226A;   ff)\tANGIOGRAPHY PACK, Model Number DYNJ47906;   gg)\tANGIO DRAPE SPEC PROC PACK-LF, Model Number DYNJ47951A;   hh)\tMH HOOD CARDIAC ANGIO, Model Number DYNJ49884F;   ii)\tANGIO PACK, Model Number DYNJ50624A;   jj)\tANGIO PACK, Model Number DYNJ51239A;  kk)\tANGIO TRAY, Model Number DYNJ52121;   ll)\tANGIO PACK-LF, Model Number DYNJ52898C;   mm)\tANGIOGRAPHY PACK, Model Number DYNJ55252B;   nn)\tANGIOGRAPHY PACK, Model Number DYNJ57498;   oo)\tPERCUTANEOUS ANGIO PACK-LF, Model Number DYNJ57645B;   pp)\tGENERAL ANGIO PACK, Model Number DYNJ57760B;   qq)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792A;   rr)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792B;   ss)\tANGIO PACK, Model Number DYNJ58126A;   tt)\tHH ANGIO PACK, Model Number DYNJ59465B;   uu)\tOR ANGIO PACK, Model Number DYNJ60319A;   vv)\tANGIO PACK 2-A, Model Number DYNJ60507A;   ww)\tFEMORAL ANGIOGRAPY SET UP, Model Number DYNJ61015B;   xx)\tANGIO PACK, Model Number DYNJ62299;   yy)\tCLOVIS CATH LAB PACK, Model Number DYNJ62379;   zz)\tANGIO PACK, Model Number DYNJ62544;   aaa)\tANGIO TRAY W/CHLORAPREP, Model Number DYNJ62742;   bbb)\tOR ANGIO PAC\t, Model Number DYNJ63976A;   ccc)\tSUNSHINE PAC\t, Model Number DYNJ64830;   ddd)\tANGIO PAC\t, Model Number DYNJ65043A;   eee)\tCATH LAB PAC\t, Model Number DYNJ65185;   fff)\tANGIOGRAPHY PACK, Model Number DYNJ65190C;   ggg)\tPACK,BASIC ANGIO, Model Number DYNJ65482A;   hhh)\tANGIO PACK, Model Number DYNJ66398B;   iii)\tANGIOGRAPHY PACK, Model Number DYNJ66476;   jjj)\tSURGERY ANGIO PACK-LF, Model Number DYNJ66500;   kkk)\tOR ANGIOGRAPHY PACK, Model Number DYNJ67245;   lll)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJ68065A;   mmm)\tANGIO TRAY, Model Number DYNJ68758;   nnn)\tANGIO, Model Number\tDYNJ902507B;   ooo)\tANGIOGRAPHY PACK, Model Number DYNJC2371G;   ppp)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJT2344B;   qqq)\tPEDI ANGIO PACK-LF, Model Number PHS41743D (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.",
  "license": "https://creativecommons.org/publicdomain/zero/1.0/",
  "isAccessibleForFree": true,
  "isPartOf": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
  "rdfs:isDefinedBy": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native",
  "seeAlso": "https://agenticu.ryanjhunter.workers.dev/commons/the-research-object",
  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
    "url": "https://open.fda.gov/apis/drug/enforcement/",
    "creator": {
      "@type": "schema:GovernmentOrganization",
      "name": "U.S. Food & Drug Administration"
    }
  },
  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2159-2023&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tANGIOGRAPHY DRP PK PEDI CATH, Model Number 00-401318M;   b)\tANGIOGRAPHY OR, Model Number CDS984944C;   c)\tANGIOGRAM, Model Number DYNJ0149444M;   d)\tEP LAB DEVICE PACK-LF, Model Number DYNJ0160556D;   e)\tVASCULAR ANGIO PACK-LF, Model Number DYNJ0201109AG;   f)\tANGIO PACK-LF, Model Number DYNJ0373279M;   g)\tVISCERAL ANGIOGRAM PACK-LF, Model Number DYNJ0429121I;   h)\tIPMC ANGIOGRAPHY PACK-LF, Model Number DYNJ0806254D;  i)\tANGIOGRAPHY PACK-LF, Model Number DYNJ0854485T;   j)\tANGIO DRAPE PACK, Model Number DYNJ17624B;   k)\tDEPAUL ANGIO PACK, Model Number DYNJ19939M;   l)\tEP ANGIOGRAPHY PACK, Model Number DYNJ24225K;   m)\tANGIOGRAPHY DRAPE PACK-LF, Model Number\tDYNJ28067G;   n)\tDASHTI-YAO NEURO ANGIO-LF, Model Number DYNJ33457C;   o)\tANGIOGRAM TRAY, Model Number DYNJ33638K;   p)\tANGIO PACK, Model Number DYNJ34361;   q)\tANGIO/PICC PACK, Model Number DYNJ36049;   r)\tIR MINOR ANGIO PACK, Model Number\tDYNJ37665B;   s)\tANGIO LEFT HEART PACK, Model Number DYNJ40632C;   t)\tMV-IR ANGIO DRAPE PACK-LF, Model Number DYNJ41553D;   u)\tCUSTOM ANGIO TRAY, Model Number DYNJ41649F;   v)\tFS ANGIO, Model Number DYNJ42499C;   w)\tANGIO PACK, Model Number DYNJ42903B;   x)\tANGIO PACK, Model Number DYNJ43661B;   y)\tANGIOGRAPHY PACK, Model Number DYNJ44293D;   z)\tANGIO DRAPE PACK, Model Number DYNJ44320F;   aa)\tANGIOGRAM PACK, Model Number DYNJ45007;   bb)\tANGIO BASIN SET, Model Number DYNJ46043F;   cc)\tANGIO TRAY, Model Number DYNJ46153B;   dd)\tANGIOGRAM PACK, Model Number DYNJ47004C;   ee)\tANGIO PACK, Model Number DYNJ47226A;   ff)\tANGIOGRAPHY PACK, Model Number DYNJ47906;   gg)\tANGIO DRAPE SPEC PROC PACK-LF, Model Number DYNJ47951A;   hh)\tMH HOOD CARDIAC ANGIO, Model Number DYNJ49884F;   ii)\tANGIO PACK, Model Number DYNJ50624A;   jj)\tANGIO PACK, Model Number DYNJ51239A;  kk)\tANGIO TRAY, Model Number DYNJ52121;   ll)\tANGIO PACK-LF, Model Number DYNJ52898C;   mm)\tANGIOGRAPHY PACK, Model Number DYNJ55252B;   nn)\tANGIOGRAPHY PACK, Model Number DYNJ57498;   oo)\tPERCUTANEOUS ANGIO PACK-LF, Model Number DYNJ57645B;   pp)\tGENERAL ANGIO PACK, Model Number DYNJ57760B;   qq)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792A;   rr)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792B;   ss)\tANGIO PACK, Model Number DYNJ58126A;   tt)\tHH ANGIO PACK, Model Number DYNJ59465B;   uu)\tOR ANGIO PACK, Model Number DYNJ60319A;   vv)\tANGIO PACK 2-A, Model Number DYNJ60507A;   ww)\tFEMORAL ANGIOGRAPY SET UP, Model Number DYNJ61015B;   xx)\tANGIO PACK, Model Number DYNJ62299;   yy)\tCLOVIS CATH LAB PACK, Model Number DYNJ62379;   zz)\tANGIO PACK, Model Number DYNJ62544;   aaa)\tANGIO TRAY W/CHLORAPREP, Model Number DYNJ62742;   bbb)\tOR ANGIO PAC\t, Model Number DYNJ63976A;   ccc)\tSUNSHINE PAC\t, Model Number DYNJ64830;   ddd)\tANGIO PAC\t, Model Number DYNJ65043A;   eee)\tCATH LAB PAC\t, Model Number DYNJ65185;   fff)\tANGIOGRAPHY PACK, Model Number DYNJ65190C;   ggg)\tPACK,BASIC ANGIO, Model Number DYNJ65482A;   hhh)\tANGIO PACK, Model Number DYNJ66398B;   iii)\tANGIOGRAPHY PACK, Model Number DYNJ66476;   jjj)\tSURGERY ANGIO PACK-LF, Model Number DYNJ66500;   kkk)\tOR ANGIOGRAPHY PACK, Model Number DYNJ67245;   lll)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJ68065A;   mmm)\tANGIO TRAY, Model Number DYNJ68758;   nnn)\tANGIO, Model Number\tDYNJ902507B;   ooo)\tANGIOGRAPHY PACK, Model Number DYNJC2371G;   ppp)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJT2344B;   qqq)\tPEDI ANGIO PACK-LF, Model Number PHS41743D",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2159-2023/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2159-2023: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tANGIOGRAPHY DRP PK PEDI CATH, Model Number 00-401318M;   b)\tANGIOGRAPHY OR, Model Number CDS984944C;   c)\tANGIOGRAM, Model Number DYNJ0149444M;   d)\tEP LAB DEVICE PACK-LF, Model Number DYNJ0160556D;   e)\tVASCULAR ANGIO PACK-LF, Model Number DYNJ0201109AG;   f)\tANGIO PACK-LF, Model Number DYNJ0373279M;   g)\tVISCERAL ANGIOGRAM PACK-LF, Model Number DYNJ0429121I;   h)\tIPMC ANGIOGRAPHY PACK-LF, Model Number DYNJ0806254D;  i)\tANGIOGRAPHY PACK-LF, Model Number DYNJ0854485T;   j)\tANGIO DRAPE PACK, Model Number DYNJ17624B;   k)\tDEPAUL ANGIO PACK, Model Number DYNJ19939M;   l)\tEP ANGIOGRAPHY PACK, Model Number DYNJ24225K;   m)\tANGIOGRAPHY DRAPE PACK-LF, Model Number\tDYNJ28067G;   n)\tDASHTI-YAO NEURO ANGIO-LF, Model Number DYNJ33457C;   o)\tANGIOGRAM TRAY, Model Number DYNJ33638K;   p)\tANGIO PACK, Model Number DYNJ34361;   q)\tANGIO/PICC PACK, Model Number DYNJ36049;   r)\tIR MINOR ANGIO PACK, Model Number\tDYNJ37665B;   s)\tANGIO LEFT HEART PACK, Model Number DYNJ40632C;   t)\tMV-IR ANGIO DRAPE PACK-LF, Model Number DYNJ41553D;   u)\tCUSTOM ANGIO TRAY, Model Number DYNJ41649F;   v)\tFS ANGIO, Model Number DYNJ42499C;   w)\tANGIO PACK, Model Number DYNJ42903B;   x)\tANGIO PACK, Model Number DYNJ43661B;   y)\tANGIOGRAPHY PACK, Model Number DYNJ44293D;   z)\tANGIO DRAPE PACK, Model Number DYNJ44320F;   aa)\tANGIOGRAM PACK, Model Number DYNJ45007;   bb)\tANGIO BASIN SET, Model Number DYNJ46043F;   cc)\tANGIO TRAY, Model Number DYNJ46153B;   dd)\tANGIOGRAM PACK, Model Number DYNJ47004C;   ee)\tANGIO PACK, Model Number DYNJ47226A;   ff)\tANGIOGRAPHY PACK, Model Number DYNJ47906;   gg)\tANGIO DRAPE SPEC PROC PACK-LF, Model Number DYNJ47951A;   hh)\tMH HOOD CARDIAC ANGIO, Model Number DYNJ49884F;   ii)\tANGIO PACK, Model Number DYNJ50624A;   jj)\tANGIO PACK, Model Number DYNJ51239A;  kk)\tANGIO TRAY, Model Number DYNJ52121;   ll)\tANGIO PACK-LF, Model Number DYNJ52898C;   mm)\tANGIOGRAPHY PACK, Model Number DYNJ55252B;   nn)\tANGIOGRAPHY PACK, Model Number DYNJ57498;   oo)\tPERCUTANEOUS ANGIO PACK-LF, Model Number DYNJ57645B;   pp)\tGENERAL ANGIO PACK, Model Number DYNJ57760B;   qq)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792A;   rr)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792B;   ss)\tANGIO PACK, Model Number DYNJ58126A;   tt)\tHH ANGIO PACK, Model Number DYNJ59465B;   uu)\tOR ANGIO PACK, Model Number DYNJ60319A;   vv)\tANGIO PACK 2-A, Model Number DYNJ60507A;   ww)\tFEMORAL ANGIOGRAPY SET UP, Model Number DYNJ61015B;   xx)\tANGIO PACK, Model Number DYNJ62299;   yy)\tCLOVIS CATH LAB PACK, Model Number DYNJ62379;   zz)\tANGIO PACK, Model Number DYNJ62544;   aaa)\tANGIO TRAY W/CHLORAPREP, Model Number DYNJ62742;   bbb)\tOR ANGIO PAC\t, Model Number DYNJ63976A;   ccc)\tSUNSHINE PAC\t, Model Number DYNJ64830;   ddd)\tANGIO PAC\t, Model Number DYNJ65043A;   eee)\tCATH LAB PAC\t, Model Number DYNJ65185;   fff)\tANGIOGRAPHY PACK, Model Number DYNJ65190C;   ggg)\tPACK,BASIC ANGIO, Model Number DYNJ65482A;   hhh)\tANGIO PACK, Model Number DYNJ66398B;   iii)\tANGIOGRAPHY PACK, Model Number DYNJ66476;   jjj)\tSURGERY ANGIO PACK-LF, Model Number DYNJ66500;   kkk)\tOR ANGIOGRAPHY PACK, Model Number DYNJ67245;   lll)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJ68065A;   mmm)\tANGIO TRAY, Model Number DYNJ68758;   nnn)\tANGIO, Model Number\tDYNJ902507B;   ooo)\tANGIOGRAPHY PACK, Model Number DYNJC2371G;   ppp)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJT2344B;   qqq)\tPEDI ANGIO PACK-LF, Model Number PHS41743D",
      "text": "The FDA logged enforcement record Z-2159-2023: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:  a)\tANGIOGRAPHY DRP PK PEDI CATH, Model Number 00-401318M;   b)\tANGIOGRAPHY OR, Model Number CDS984944C;   c)\tANGIOGRAM, Model Number DYNJ0149444M;   d)\tEP LAB DEVICE PACK-LF, Model Number DYNJ0160556D;   e)\tVASCULAR ANGIO PACK-LF, Model Number DYNJ0201109AG;   f)\tANGIO PACK-LF, Model Number DYNJ0373279M;   g)\tVISCERAL ANGIOGRAM PACK-LF, Model Number DYNJ0429121I;   h)\tIPMC ANGIOGRAPHY PACK-LF, Model Number DYNJ0806254D;  i)\tANGIOGRAPHY PACK-LF, Model Number DYNJ0854485T;   j)\tANGIO DRAPE PACK, Model Number DYNJ17624B;   k)\tDEPAUL ANGIO PACK, Model Number DYNJ19939M;   l)\tEP ANGIOGRAPHY PACK, Model Number DYNJ24225K;   m)\tANGIOGRAPHY DRAPE PACK-LF, Model Number\tDYNJ28067G;   n)\tDASHTI-YAO NEURO ANGIO-LF, Model Number DYNJ33457C;   o)\tANGIOGRAM TRAY, Model Number DYNJ33638K;   p)\tANGIO PACK, Model Number DYNJ34361;   q)\tANGIO/PICC PACK, Model Number DYNJ36049;   r)\tIR MINOR ANGIO PACK, Model Number\tDYNJ37665B;   s)\tANGIO LEFT HEART PACK, Model Number DYNJ40632C;   t)\tMV-IR ANGIO DRAPE PACK-LF, Model Number DYNJ41553D;   u)\tCUSTOM ANGIO TRAY, Model Number DYNJ41649F;   v)\tFS ANGIO, Model Number DYNJ42499C;   w)\tANGIO PACK, Model Number DYNJ42903B;   x)\tANGIO PACK, Model Number DYNJ43661B;   y)\tANGIOGRAPHY PACK, Model Number DYNJ44293D;   z)\tANGIO DRAPE PACK, Model Number DYNJ44320F;   aa)\tANGIOGRAM PACK, Model Number DYNJ45007;   bb)\tANGIO BASIN SET, Model Number DYNJ46043F;   cc)\tANGIO TRAY, Model Number DYNJ46153B;   dd)\tANGIOGRAM PACK, Model Number DYNJ47004C;   ee)\tANGIO PACK, Model Number DYNJ47226A;   ff)\tANGIOGRAPHY PACK, Model Number DYNJ47906;   gg)\tANGIO DRAPE SPEC PROC PACK-LF, Model Number DYNJ47951A;   hh)\tMH HOOD CARDIAC ANGIO, Model Number DYNJ49884F;   ii)\tANGIO PACK, Model Number DYNJ50624A;   jj)\tANGIO PACK, Model Number DYNJ51239A;  kk)\tANGIO TRAY, Model Number DYNJ52121;   ll)\tANGIO PACK-LF, Model Number DYNJ52898C;   mm)\tANGIOGRAPHY PACK, Model Number DYNJ55252B;   nn)\tANGIOGRAPHY PACK, Model Number DYNJ57498;   oo)\tPERCUTANEOUS ANGIO PACK-LF, Model Number DYNJ57645B;   pp)\tGENERAL ANGIO PACK, Model Number DYNJ57760B;   qq)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792A;   rr)\tENSEMBLE ANGIOGRAPHIE-LF, Model Number DYNJ57792B;   ss)\tANGIO PACK, Model Number DYNJ58126A;   tt)\tHH ANGIO PACK, Model Number DYNJ59465B;   uu)\tOR ANGIO PACK, Model Number DYNJ60319A;   vv)\tANGIO PACK 2-A, Model Number DYNJ60507A;   ww)\tFEMORAL ANGIOGRAPY SET UP, Model Number DYNJ61015B;   xx)\tANGIO PACK, Model Number DYNJ62299;   yy)\tCLOVIS CATH LAB PACK, Model Number DYNJ62379;   zz)\tANGIO PACK, Model Number DYNJ62544;   aaa)\tANGIO TRAY W/CHLORAPREP, Model Number DYNJ62742;   bbb)\tOR ANGIO PAC\t, Model Number DYNJ63976A;   ccc)\tSUNSHINE PAC\t, Model Number DYNJ64830;   ddd)\tANGIO PAC\t, Model Number DYNJ65043A;   eee)\tCATH LAB PAC\t, Model Number DYNJ65185;   fff)\tANGIOGRAPHY PACK, Model Number DYNJ65190C;   ggg)\tPACK,BASIC ANGIO, Model Number DYNJ65482A;   hhh)\tANGIO PACK, Model Number DYNJ66398B;   iii)\tANGIOGRAPHY PACK, Model Number DYNJ66476;   jjj)\tSURGERY ANGIO PACK-LF, Model Number DYNJ66500;   kkk)\tOR ANGIOGRAPHY PACK, Model Number DYNJ67245;   lll)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJ68065A;   mmm)\tANGIO TRAY, Model Number DYNJ68758;   nnn)\tANGIO, Model Number\tDYNJ902507B;   ooo)\tANGIOGRAPHY PACK, Model Number DYNJC2371G;   ppp)\tANGIOGRAPHY DRAPE PACK, Model Number DYNJT2344B;   qqq)\tPEDI ANGIO PACK-LF, Model Number PHS41743D — reason: Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-05-18. Affected lots/codes: all lots within expiry, distributed from Medline between December 2017 - May 2023:   a) Model Number 00-401318M, UDI/DI (EA)10193489348750, UDI/DI (CS)40193489348751 b) Model Number CDS984944C, UDI/DI (EA)10889942172955, UDI/DI (CS)40889942172956 c) Model Number DYNJ0149444M, UDI/DI (EA)10193489432824, UDI/DI (CS)40193489432825 d) Model Number DYNJ0160556D, UDI/DI (EA)10193489207552, UDI/DI (CS)40193489207553 e) Model Number DYNJ0201109AG, UDI/DI (EA)10193489497267, UDI/DI (CS)40193489497268 f) Model Number DYNJ0373279M, UDI/DI (EA)10193489519020, UDI/DI (CS)40193489519021 g) Model Number DYNJ0429121I, UDI/DI (EA)10193489897494, UDI/DI (CS)40193489897495 h) Model Number DYNJ0806254D, UDI/DI (EA)10889942471164, UDI/DI (CS)40889942471165 i) Model Number DYNJ0854485T, UDI/DI (EA)10193489864199, UDI/DI (CS)40193489864190 j) Model Number DYNJ17624B, UDI/DI (EA)10193489867299, UDI/DI (CS)40193489867290 k) Model Number DYNJ19939M, UDI/DI (EA)10193489393248, UDI/DI (CS)40193489393249 l) Model Number DYNJ24225K, UDI/DI (EA)10889942510702, UDI/DI (CS)40889942510703 m) Model Number DYNJ28067G, UDI/DI (EA)10889942744299, UDI/DI (CS)40889942744290 n) Model Number DYNJ33457C, UDI/DI (EA)10193489461800, UDI/DI (CS)40193489461801 o) Model Number DYNJ33638K, UDI/DI (EA)10193489343281, UDI/DI (CS)40193489343282 p) Model Number DYNJ34361, UDI/DI (EA)10884389348475, UDI/DI (CS)40884389348476 q) Model Number DYNJ36049, UDI/DI (EA)10884389498675, UDI/DI (CS)40884389498676 r) Model Number DYNJ37665B, UDI/DI (EA)10889942969739, UDI/DI (CS)40889942969730 s) Model Number DYNJ40632C, UDI/DI (EA)10193489461176, UDI/DI (CS)40193489461177 t) Model Number DYNJ41553D, UDI/DI (EA)10889942811335, UDI/DI (CS)40889942811336 u) Model Number DYNJ41649F, UDI/DI (EA)10193489641271, UDI/DI (CS)40193489641272 v) Model Number DYNJ42499C, UDI/DI (EA)10195327030865, UDI/DI (CS)40195327030866 w) Model Number DYNJ42903B, UDI/DI (EA)10888277798014, UDI/DI (CS)40888277798015 x) Model Number DYNJ43661B, UDI/DI (EA)10889942808700, UDI/DI (CS)40889942808701 y) Model Number DYNJ44293D, UDI/DI (EA)10193489833416, UDI/DI (CS)40193489833417 z) Model Number DYNJ44320F, UDI/DI (EA)10193489435511, UDI/DI (CS)40193489435512 aa) Model Number DYNJ45007, UDI/DI (EA)10888277085411, UDI/DI (CS)40888277085412 bb) Model Number DYNJ46043F, UDI/DI (EA)10193489856729, UDI/DI (CS)40193489856720 cc) Model Number DYNJ46153B, UDI/DI (EA)10193489853643, UDI/DI (CS)40193489853644 dd) Model Number DYNJ47004C, UDI/DI (EA)10193489696172, UDI/DI (CS)40193489696173 ee) Model Number DYNJ47226A, UDI/DI (EA)10888277561816, UDI/DI (CS)40888277561817 ff) Model Number DYNJ47906, UDI/DI (EA)10888277528376, UDI/DI (CS)40888277528377 gg) Model Number DYNJ47951A, UDI/DI (EA)10193489609844, UDI/DI (CS)40193489609845 hh) Model Number DYNJ49884F, UDI/DI (EA)10193489469578, UDI/DI (CS)40193489469579 ii) Model Number DYNJ50624A, UDI/DI (EA)10889942474639, UDI/DI (CS)40889942474630 jj) Model Number DYNJ51239A, UDI/DI (EA)10889942493548, UDI/DI (CS)40889942493549 kk) Model Number DYNJ52121, UDI/DI (EA)10889942243624, UDI/DI (CS)40889942243625 ll) Model Number DYNJ52898C, UDI/DI (EA)10193489876314, UDI/DI (CS)40193489876315 mm) Model Number DYNJ55252B, UDI/DI (EA)10193489870152, UDI/DI (CS)40193489870153 nn) Model Number DYNJ57498, UDI/DI (EA)10889942745746, UDI/DI (CS)40889942745747 oo) Model Number DYNJ57645B, UDI/DI (EA)10193489828658, UDI/DI (CS)40193489828659 pp) Model Number DYNJ57760B, UDI/DI (EA)10193489342581, UDI/DI (CS)40193489342582 qq) Model Number DYNJ57792A, UDI/DI (EA)10193489530896, UDI/DI (CS)40193489530897 rr) Model Number DYNJ57792B, UDI/DI (EA)10193489845945, UDI/DI (CS)40193489845946 ss) Model Number DYNJ58126A, UDI/DI (EA)10193489484755, UDI/DI (CS)40193489484756 tt) Model Number DYNJ59465B, UDI/DI (EA)10193489470932, UDI/DI (CS)40193489470933 uu) Model Number DYNJ60319A, UDI/DI (EA)10193489276299, UDI/DI (CS)40193489276290 vv) Model Number DYNJ60507A, UDI/DI (EA)10193489830552, UDI/DI (CS)40193489830553 ww) Model Number DYNJ61015B, UDI/DI (EA)10193489368888, UDI/DI (CS)40193489368889 xx) Model Number DYNJ62299, UDI/DI (EA)10193489641516, UDI/DI (CS)40193489641517 yy) Model Number DYNJ62379, UDI/DI (EA)10193489651706, UDI/DI (CS)40193489651707 zz) Model Number DYNJ62544, UDI/DI (EA)10193489666526, UDI/DI (CS)40193489666527 aaa) Model Number DYNJ62742, UDI/DI (EA)10193489685923, UDI/DI (CS)40193489685924 bbb) Model Number DYNJ63976A, UDI/DI (EA)10193489377965, UDI/DI (CS)40193489377966 ccc) Model Number DYNJ64830, UDI/DI (EA)10193489223132, UDI/DI (CS)40193489223133 ddd) Model Number DYNJ65043A, UDI/DI (EA)10193489379327, UDI/DI (CS)40193489379328 eee) Model Number DYNJ65185, UDI/DI (EA)10193489253146, UDI/DI (CS)40193489253147 fff) Model Number DYNJ65190C, UDI/DI (EA)10193489433111, UDI/DI (CS)40193489433112 ggg) Model Number DYNJ65482A, UDI/DI (EA)10193489416824, UDI/DI (CS)40193489416825 hhh) Model Number DYNJ66398B, UDI/DI (EA)10193489891928, UDI/DI (CS)40193489891929 iii) Model Number DYNJ66476, UDI/DI (EA)10193489356779, UDI/DI (CS)40193489356770 jjj) Model Number DYNJ66500, UDI/DI (EA)10193489357912, UDI/DI (CS)40193489357913 kkk) Model Number DYNJ67245, UDI/DI (EA)10193489393057, UDI/DI (CS)40193489393058 lll) Model Number DYNJ68065A, UDI/DI (EA)10193489888720, UDI/DI (CS)40193489888721 mmm) Model Number DYNJ68758, UDI/DI (EA)10193489837568, UDI/DI (CS)40193489837569 nnn) Model Number DYNJ902507B, UDI/DI (EA)10889942781188, UDI/DI (CS)40889942781189 ooo) Model Number DYNJC2371G, UDI/DI (EA)10889942494675, UDI/DI (CS)40889942494676 ppp) Model Number DYNJT2344B, UDI/DI (EA)10889942107803, UDI/DI (CS)40889942107804 qqq) Model Number PHS41743D, UDI/DI (EA)10193489453270, UDI/DI (CS)40193489453271. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
      },
      "grounding": {
        "groundingType": "SourceCitation",
        "source": "openFDA drug & device enforcement (recall) reports — U.S. FDA",
        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2159-2023&lang=eng",
        "value": "Devices recall, status Ongoing",
        "adjudicator": {
          "name": "openFDA drug & device enforcement (recall) reports — U.S. FDA",
          "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2159-2023&lang=eng"
        }
      },
      "falsifier": "A RECORD of measured/reported events (occurred=true) from openFDA drug & device enforcement (recall) reports — U.S. FDA; superseded when openFDA drug & device enforcement (recall) reports — U.S. FDA publishes its next release."
    },
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2159-2023/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2159-2023 as Class II",
      "text": "The FDA assigned this recall Class II: Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.. This is the FDA's official risk classification — its regulatory DETERMINATION of the hazard category (a verdict constituted by the FDA's recognition, occurred=FALSE), adjudged=TRUE because the FDA issued it. It is NOT a measurement of harm to any specific person.",
      "claimType": "regulatory_determination",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": false,
        "supported": true,
        "adjudged": true,
        "operative": true
      },
      "grounding": {
        "groundingType": "AdjudicativeAct",
        "source": "U.S. FDA recall classification (openFDA enforcement)",
        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2159-2023&lang=eng",
        "value": "Class II",
        "adjudicator": {
          "name": "U.S. FDA recall classification (openFDA enforcement)",
          "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-2159-2023&lang=eng"
        }
      },
      "falsifier": "occurred=FALSE: a regulatory DETERMINATION (an authority's classification/judgment) has NO material truthmaker independent of recognition — it is constituted by U.S. FDA recall classification (openFDA enforcement)'s say-so (a Searle institutional fact), not measured. adjudged=TRUE because U.S. FDA recall classification (openFDA enforcement) (an external authority) issued it. Distinct from a recorded measurement (which has an independent truthmaker) and from a modeled figure (a computed quantity, not a verdict). Challengeable; superseded if the authority reclassifies."
    },
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2159-2023/boundary",
      "@type": "schema:Claim",
      "name": "What an FDA recall is — and is NOT",
      "text": "A recall is a RECORDED FDA enforcement action — the FDA logged that a firm is removing or correcting a product, classed by the FDA's risk judgment. It does NOT establish that any specific unit is affected or caused harm; causation is not established. This record informs and compares — it is NOT medical advice and does not tell anyone to start or stop a drug or device. For a medical decision, route to the FDA recall record and a licensed pharmacist or prescriber.",
      "claimType": "interpretation",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": false,
        "supported": true,
        "adjudged": false,
        "operative": true
      },
      "grounding": {
        "groundingType": "Interpretation",
        "source": "Atlas Commons L5 boundary (enforcement-action ≠ harm causation)",
        "sourceUrl": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
        "value": "a recorded enforcement action, not proof of harm or causation; not medical advice",
        "adjudicator": null
      },
      "falsifier": "occurred=FALSE (a framing, not an event) and adjudged=FALSE (an in-house reading, not an authority's verdict) — the LOWEST-warrant claim here. A flat representation would render this identically to the official facts; the four-status does not."
    }
  ],
  "hasPart": [
    {
      "@type": "schema:ItemList",
      "name": "FDA recall details — Z-2159-2023",
      "numberOfItems": 9,
      "itemListElement": [
        {
          "@type": "schema:ListItem",
          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-2159-2023",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 3,
          "item": {
            "Field": "Classification",
            "Value": "Class II",
            "Status": "determination"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 4,
          "item": {
            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "MEDLINE INDUSTRIES, LP - Northfield",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2023-05-18",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "all lots within expiry, distributed from Medline between December 2017 - May 2023:   a) Model Number 00-401318M, UDI/DI (EA)10193489348750, UDI/DI (CS)40193489348751 b) Model Number CDS984944C, UDI/DI (EA)10889942172955, UDI/DI (CS)40889942172956 c) Model Number DYNJ0149444M, UDI/DI (EA)10193489432824, UDI/DI (CS)40193489432825 d) Model Number DYNJ0160556D, UDI/DI (EA)10193489207552, UDI/DI (CS)40193489207553 e) Model Number DYNJ0201109AG, UDI/DI (EA)10193489497267, UDI/DI (CS)40193489497268 f) Model Number DYNJ0373279M, UDI/DI (EA)10193489519020, UDI/DI (CS)40193489519021 g) Model Number DYNJ0429121I, UDI/DI (EA)10193489897494, UDI/DI (CS)40193489897495 h) Model Number DYNJ0806254D, UDI/DI (EA)10889942471164, UDI/DI (CS)40889942471165 i) Model Number DYNJ0854485T, UDI/DI (EA)10193489864199, UDI/DI (CS)40193489864190 j) Model Number DYNJ17624B, UDI/DI (EA)10193489867299, UDI/DI (CS)40193489867290 k) Model Number DYNJ19939M, UDI/DI (EA)10193489393248, UDI/DI (CS)40193489393249 l) Model Number DYNJ24225K, UDI/DI (EA)10889942510702, UDI/DI (CS)40889942510703 m) Model Number DYNJ28067G, UDI/DI (EA)10889942744299, UDI/DI (CS)40889942744290 n) Model Number DYNJ33457C, UDI/DI (EA)10193489461800, UDI/DI (CS)40193489461801 o) Model Number DYNJ33638K, UDI/DI (EA)10193489343281, UDI/DI (CS)40193489343282 p) Model Number DYNJ34361, UDI/DI (EA)10884389348475, UDI/DI (CS)40884389348476 q) Model Number DYNJ36049, UDI/DI (EA)10884389498675, UDI/DI (CS)40884389498676 r) Model Number DYNJ37665B, UDI/DI (EA)10889942969739, UDI/DI (CS)40889942969730 s) Model Number DYNJ40632C, UDI/DI (EA)10193489461176, UDI/DI (CS)40193489461177 t) Model Number DYNJ41553D, UDI/DI (EA)10889942811335, UDI/DI (CS)40889942811336 u) Model Number DYNJ41649F, UDI/DI (EA)10193489641271, UDI/DI (CS)40193489641272 v) Model Number DYNJ42499C, UDI/DI (EA)10195327030865, UDI/DI (CS)40195327030866 w) Model Number DYNJ42903B, UDI/DI (EA)10888277798014, UDI/DI (CS)40888277798015 x) Model Number DYNJ43661B, UDI/DI (EA)10889942808700, UDI/DI (CS)40889942808701 y) Model Number DYNJ44293D, UDI/DI (EA)10193489833416, UDI/DI (CS)40193489833417 z) Model Number DYNJ44320F, UDI/DI (EA)10193489435511, UDI/DI (CS)40193489435512 aa) Model Number DYNJ45007, UDI/DI (EA)10888277085411, UDI/DI (CS)40888277085412 bb) Model Number DYNJ46043F, UDI/DI (EA)10193489856729, UDI/DI (CS)40193489856720 cc) Model Number DYNJ46153B, UDI/DI (EA)10193489853643, UDI/DI (CS)40193489853644 dd) Model Number DYNJ47004C, UDI/DI (EA)10193489696172, UDI/DI (CS)40193489696173 ee) Model Number DYNJ47226A, UDI/DI (EA)10888277561816, UDI/DI (CS)40888277561817 ff) Model Number DYNJ47906, UDI/DI (EA)10888277528376, UDI/DI (CS)40888277528377 gg) Model Number DYNJ47951A, UDI/DI (EA)10193489609844, UDI/DI (CS)40193489609845 hh) Model Number DYNJ49884F, UDI/DI (EA)10193489469578, UDI/DI (CS)40193489469579 ii) Model Number DYNJ50624A, UDI/DI (EA)10889942474639, UDI/DI (CS)40889942474630 jj) Model Number DYNJ51239A, UDI/DI (EA)10889942493548, UDI/DI (CS)40889942493549 kk) Model Number DYNJ52121, UDI/DI (EA)10889942243624, UDI/DI (CS)40889942243625 ll) Model Number DYNJ52898C, UDI/DI (EA)10193489876314, UDI/DI (CS)40193489876315 mm) Model Number DYNJ55252B, UDI/DI (EA)10193489870152, UDI/DI (CS)40193489870153 nn) Model Number DYNJ57498, UDI/DI (EA)10889942745746, UDI/DI (CS)40889942745747 oo) Model Number DYNJ57645B, UDI/DI (EA)10193489828658, UDI/DI (CS)40193489828659 pp) Model Number DYNJ57760B, UDI/DI (EA)10193489342581, UDI/DI (CS)40193489342582 qq) Model Number DYNJ57792A, UDI/DI (EA)10193489530896, UDI/DI (CS)40193489530897 rr) Model Number DYNJ57792B, UDI/DI (EA)10193489845945, UDI/DI (CS)40193489845946 ss) Model Number DYNJ58126A, UDI/DI (EA)10193489484755, UDI/DI (CS)40193489484756 tt) Model Number DYNJ59465B, UDI/DI (EA)10193489470932, UDI/DI (CS)40193489470933 uu) Model Number DYNJ60319A, UDI/DI (EA)10193489276299, UDI/DI (CS)40193489276290 vv) Model Number DYNJ60507A, UDI/DI (EA)10193489830552, UDI/DI (CS)40193489830553 ww) Model Number DYNJ61015B, UDI/DI (EA)10193489368888, UDI/DI (CS)40193489368889 xx) Model Number DYNJ62299, UDI/DI (EA)10193489641516, UDI/DI (CS)40193489641517 yy) Model Number DYNJ62379, UDI/DI (EA)10193489651706, UDI/DI (CS)40193489651707 zz) Model Number DYNJ62544, UDI/DI (EA)10193489666526, UDI/DI (CS)40193489666527 aaa) Model Number DYNJ62742, UDI/DI (EA)10193489685923, UDI/DI (CS)40193489685924 bbb) Model Number DYNJ63976A, UDI/DI (EA)10193489377965, UDI/DI (CS)40193489377966 ccc) Model Number DYNJ64830, UDI/DI (EA)10193489223132, UDI/DI (CS)40193489223133 ddd) Model Number DYNJ65043A, UDI/DI (EA)10193489379327, UDI/DI (CS)40193489379328 eee) Model Number DYNJ65185, UDI/DI (EA)10193489253146, UDI/DI (CS)40193489253147 fff) Model Number DYNJ65190C, UDI/DI (EA)10193489433111, UDI/DI (CS)40193489433112 ggg) Model Number DYNJ65482A, UDI/DI (EA)10193489416824, UDI/DI (CS)40193489416825 hhh) Model Number DYNJ66398B, UDI/DI (EA)10193489891928, UDI/DI (CS)40193489891929 iii) Model Number DYNJ66476, UDI/DI (EA)10193489356779, UDI/DI (CS)40193489356770 jjj) Model Number DYNJ66500, UDI/DI (EA)10193489357912, UDI/DI (CS)40193489357913 kkk) Model Number DYNJ67245, UDI/DI (EA)10193489393057, UDI/DI (CS)40193489393058 lll) Model Number DYNJ68065A, UDI/DI (EA)10193489888720, UDI/DI (CS)40193489888721 mmm) Model Number DYNJ68758, UDI/DI (EA)10193489837568, UDI/DI (CS)40193489837569 nnn) Model Number DYNJ902507B, UDI/DI (EA)10889942781188, UDI/DI (CS)40889942781189 ooo) Model Number DYNJC2371G, UDI/DI (EA)10889942494675, UDI/DI (CS)40889942494676 ppp) Model Number DYNJT2344B, UDI/DI (EA)10889942107803, UDI/DI (CS)40889942107804 qqq) Model Number PHS41743D, UDI/DI (EA)10193489453270, UDI/DI (CS)40193489453271",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide Distribution: US (Nationwide) and OUS (foreign) United Arab Emirates, Singapore, Lebanon, China Qatar, Costa Rica, India, Canada, Panama & Saudi Arabia.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}