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  "name": "Centurion Kits, trays, and packs labeled as follows:    a) A C DAILY WET KIT, REF DM405A;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640;   c) DAILY DRIVELINE MGMT SYSTEM, REF DM600;   d) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   e) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   f) DRESSING CHANGE TRAY WITHOUT DRESSING, REF DT21465B;   g) DRIVELINE MANAGEMENT SYSTEM, REF DT18905;   h) DRIVELINE MANAGEMENT SYSTEM-DAILY, REF DM610;   i) DRIVELINE MGMT TRAY W/O ANCHOR, REF DT18210;   j) DRIVELINE MGMT. KIT WITH SILVER ALGINATE, REF DT18695A;   k) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   l) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   m) LVAD DRIVELINE MGMT KIT, SENSITIVE SKIN, REF DT19005A;   n) LVAD MAINTENANCE KIT - LESS THAN 6 MOS., REF DM1060;   o) LVAD SENSITIVE KIT, REF DM525A;   p) MMC DAILY DRIVELINE MGMT KIT, REF DM850;   q) PATIENT DRESSING CHANGE  KIT SW, REF DT17355;   r) PEDIATRIC PORT ACCESS BUNDLE, REF DT19835B;   s) PORT ACCESS KIT, REF DT22575A;   t) PORT ACCESS TRAY, REF DT20845B;   u) PORT DRESSING  CHANGE TRAY, REF DT20885B;   v) PORT DRESSING CHANGE KIT, REF DT21585B;   w) PORT DRESSING CHANGE KIT, REF DYNDC2815A;   x) PORT KIT, REF DT22270A;   y) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   z) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   aa) VAD DRESSING CHANGE TRAY, REF DM875;   bb) VAD DRESSING CHANGE TRAY, REF DM875;   cc) VAD DRIVELINE MANAGEMENT KIT HW, REF DM1105",
  "description": "FDA recall Z-1136-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling Centurion Kits, trays, and packs labeled as follows:    a) A C DAILY WET KIT, REF DM405A;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640;   c) DAILY DRIVELINE MGMT SYSTEM, REF DM600;   d) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   e) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   f) DRESSING CHANGE TRAY WITHOUT DRESSING, REF DT21465B;   g) DRIVELINE MANAGEMENT SYSTEM, REF DT18905;   h) DRIVELINE MANAGEMENT SYSTEM-DAILY, REF DM610;   i) DRIVELINE MGMT TRAY W/O ANCHOR, REF DT18210;   j) DRIVELINE MGMT. KIT WITH SILVER ALGINATE, REF DT18695A;   k) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   l) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   m) LVAD DRIVELINE MGMT KIT, SENSITIVE SKIN, REF DT19005A;   n) LVAD MAINTENANCE KIT - LESS THAN 6 MOS., REF DM1060;   o) LVAD SENSITIVE KIT, REF DM525A;   p) MMC DAILY DRIVELINE MGMT KIT, REF DM850;   q) PATIENT DRESSING CHANGE  KIT SW, REF DT17355;   r) PEDIATRIC PORT ACCESS BUNDLE, REF DT19835B;   s) PORT ACCESS KIT, REF DT22575A;   t) PORT ACCESS TRAY, REF DT20845B;   u) PORT DRESSING  CHANGE TRAY, REF DT20885B;   v) PORT DRESSING CHANGE KIT, REF DT21585B;   w) PORT DRESSING CHANGE KIT, REF DYNDC2815A;   x) PORT KIT, REF DT22270A;   y) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   z) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   aa) VAD DRESSING CHANGE TRAY, REF DM875;   bb) VAD DRESSING CHANGE TRAY, REF DM875;   cc) VAD DRIVELINE MANAGEMENT KIT HW, REF DM1105 (Devices, Class I). 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.",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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    "@type": "schema:MedicalDevice",
    "name": "Centurion Kits, trays, and packs labeled as follows:    a) A C DAILY WET KIT, REF DM405A;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640;   c) DAILY DRIVELINE MGMT SYSTEM, REF DM600;   d) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   e) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   f) DRESSING CHANGE TRAY WITHOUT DRESSING, REF DT21465B;   g) DRIVELINE MANAGEMENT SYSTEM, REF DT18905;   h) DRIVELINE MANAGEMENT SYSTEM-DAILY, REF DM610;   i) DRIVELINE MGMT TRAY W/O ANCHOR, REF DT18210;   j) DRIVELINE MGMT. KIT WITH SILVER ALGINATE, REF DT18695A;   k) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   l) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   m) LVAD DRIVELINE MGMT KIT, SENSITIVE SKIN, REF DT19005A;   n) LVAD MAINTENANCE KIT - LESS THAN 6 MOS., REF DM1060;   o) LVAD SENSITIVE KIT, REF DM525A;   p) MMC DAILY DRIVELINE MGMT KIT, REF DM850;   q) PATIENT DRESSING CHANGE  KIT SW, REF DT17355;   r) PEDIATRIC PORT ACCESS BUNDLE, REF DT19835B;   s) PORT ACCESS KIT, REF DT22575A;   t) PORT ACCESS TRAY, REF DT20845B;   u) PORT DRESSING  CHANGE TRAY, REF DT20885B;   v) PORT DRESSING CHANGE KIT, REF DT21585B;   w) PORT DRESSING CHANGE KIT, REF DYNDC2815A;   x) PORT KIT, REF DT22270A;   y) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   z) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   aa) VAD DRESSING CHANGE TRAY, REF DM875;   bb) VAD DRESSING CHANGE TRAY, REF DM875;   cc) VAD DRIVELINE MANAGEMENT KIT HW, REF DM1105",
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1136-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1136-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling Centurion Kits, trays, and packs labeled as follows:    a) A C DAILY WET KIT, REF DM405A;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640;   c) DAILY DRIVELINE MGMT SYSTEM, REF DM600;   d) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   e) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   f) DRESSING CHANGE TRAY WITHOUT DRESSING, REF DT21465B;   g) DRIVELINE MANAGEMENT SYSTEM, REF DT18905;   h) DRIVELINE MANAGEMENT SYSTEM-DAILY, REF DM610;   i) DRIVELINE MGMT TRAY W/O ANCHOR, REF DT18210;   j) DRIVELINE MGMT. KIT WITH SILVER ALGINATE, REF DT18695A;   k) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   l) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   m) LVAD DRIVELINE MGMT KIT, SENSITIVE SKIN, REF DT19005A;   n) LVAD MAINTENANCE KIT - LESS THAN 6 MOS., REF DM1060;   o) LVAD SENSITIVE KIT, REF DM525A;   p) MMC DAILY DRIVELINE MGMT KIT, REF DM850;   q) PATIENT DRESSING CHANGE  KIT SW, REF DT17355;   r) PEDIATRIC PORT ACCESS BUNDLE, REF DT19835B;   s) PORT ACCESS KIT, REF DT22575A;   t) PORT ACCESS TRAY, REF DT20845B;   u) PORT DRESSING  CHANGE TRAY, REF DT20885B;   v) PORT DRESSING CHANGE KIT, REF DT21585B;   w) PORT DRESSING CHANGE KIT, REF DYNDC2815A;   x) PORT KIT, REF DT22270A;   y) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   z) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   aa) VAD DRESSING CHANGE TRAY, REF DM875;   bb) VAD DRESSING CHANGE TRAY, REF DM875;   cc) VAD DRIVELINE MANAGEMENT KIT HW, REF DM1105",
      "text": "The FDA logged enforcement record Z-1136-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Centurion Kits, trays, and packs labeled as follows:    a) A C DAILY WET KIT, REF DM405A;   b) BWH DAILY DRIVELINE MGMT KIT, REF DM640;   c) DAILY DRIVELINE MGMT SYSTEM, REF DM600;   d) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   e) DAILY MAINTENANCE SYSTEM LVAD, REF DM870A;   f) DRESSING CHANGE TRAY WITHOUT DRESSING, REF DT21465B;   g) DRIVELINE MANAGEMENT SYSTEM, REF DT18905;   h) DRIVELINE MANAGEMENT SYSTEM-DAILY, REF DM610;   i) DRIVELINE MGMT TRAY W/O ANCHOR, REF DT18210;   j) DRIVELINE MGMT. KIT WITH SILVER ALGINATE, REF DT18695A;   k) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   l) LVAD DAILY PATIENT CHANGE KIT, REF DM630;   m) LVAD DRIVELINE MGMT KIT, SENSITIVE SKIN, REF DT19005A;   n) LVAD MAINTENANCE KIT - LESS THAN 6 MOS., REF DM1060;   o) LVAD SENSITIVE KIT, REF DM525A;   p) MMC DAILY DRIVELINE MGMT KIT, REF DM850;   q) PATIENT DRESSING CHANGE  KIT SW, REF DT17355;   r) PEDIATRIC PORT ACCESS BUNDLE, REF DT19835B;   s) PORT ACCESS KIT, REF DT22575A;   t) PORT ACCESS TRAY, REF DT20845B;   u) PORT DRESSING  CHANGE TRAY, REF DT20885B;   v) PORT DRESSING CHANGE KIT, REF DT21585B;   w) PORT DRESSING CHANGE KIT, REF DYNDC2815A;   x) PORT KIT, REF DT22270A;   y) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   z) UOU LVAD DRIVELINE MGMT COMPLICATIONS, REF DM330A;   aa) VAD DRESSING CHANGE TRAY, REF DM875;   bb) VAD DRESSING CHANGE TRAY, REF DM875;   cc) VAD DRIVELINE MANAGEMENT KIT HW, REF DM1105 — reason: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components):  0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-11-15. Affected lots/codes: a) REF DM405A, UDI/DI 00653160322217 (case), 10653160322214 (unit), Lot Numbers: 2022042580, 2022070580, 2022071180, 2022071880, 2022072580, 2022080180, 2023040380, 2023050180, 2023073180, 2023102380;    b) REF DM640, UDI/DI 00653160289602 (case), 10653160289609 (unit), Lot Numbers:  2022041390;   c) REF DM600, UDI/DI 00653160352610 (case), 10653160352617 (unit), Lot Numbers:  2022041880, 2023081480;   d) REF DM870A, UDI/DI 00653160348217 (case), 10653160348214 (unit), Lot Numbers: 2022020780;    e) REF DM870A, UDI/DI 00653160352382 (case), 10653160352389 (unit), Lot Numbers:   2022041880;   f) REF DT21465B, UDI/DI 00653160350005 (case), 10653160350002 (unit), Lot Numbers: 2022012550, 2022032880, 2022032980, 2022082280;    g) REF DT18905, UDI/DI 00653160275063 (case), 10653160275060 (unit), Lot Numbers:  2022040590, 2022041390, 2022081990, 2023011290, 2023012490, 2023051190, 2023061290, 2023081590, 2023101790;   h) REF DM610, UDI/DI 00653160294002 (case), 10653160294009 (unit), Lot Numbers:  2022050980, 2022072580, 2022072680, 2022080180, 2022080880, 2022081580, 2023050880, 2023061280, 2023072480, 2023081480, 2023082880;   i) REF DT18210, UDI/DI 00653160352658 (case), 10653160352655 (unit), Lot Numbers: 2022042290;    j) REF DT18695A, UDI/DI 00653160315127 (case), 10653160315124 (unit), Lot Numbers: 2022042790, 2022103190, 2023012790, 2023032490, 2023032890, 2023052690, 2023072890, 2023092190;   k) REF DM630, UDI/DI 00653160288568 (case), 10653160288565 (unit), Lot Numbers:  2022033190;   l) REF DM630, UDI/DI 00653160352450 (case), 10653160352457 (unit), Lot Numbers:  2022050590, 2022111790, 2023011990, 2023031590, 2023042490, 2023062690, 2023081490;   m) REF DT19005A, UDI/DI 00653160349801 (case), 10653160349808 (unit), Lot Numbers:   2022050980;     n) REF DM1060, UDI/DI 00653160352443 (case), 10653160352440 (unit), Lot Numbers:  2022050280, 2023070380, 2023082180, 2023082880, 2023101680;   o) REF DM525A, UDI/DI 00653160352511 (case), 10653160352518 (unit), Lot Numbers:  2022042580, 2022080180, 2022112880, 2022112980;   p) REF DM850, UDI/DI 00653160307047 (case), 10653160307044 (unit), Lot Numbers: 2022040490;    q) REF DT17355, UDI/DI 00653160265170 (case), 10653160265177 (unit), Lot Numbers:  2022082290, 2022090190, 2022112990, 2023012490, 2023042090, 2023070690, 2023073190, 2023081190;   r) REF DT19835B, UDI/DI 00653160350128 (case), 10653160350125 (unit), Lot Numbers:  2022021150, 2022022250;   s) REF DT22575A, UDI/DI 00653160349825 (case), 10653160349822 (unit), Lot Numbers: 2022011350, 2022052380, 2022052480, 2022052580;    t) REF DT20845B, UDI/DI 00653160348842 (case), 10653160348849 (unit), Lot Numbers: 2022010750, 2022031450;    u) REF DT20885B, UDI/DI 00653160348422 (case), 10653160348429 (unit), Lot Numbers:  2022052380;   v) REF DT21585B, UDI/DI 00653160351439 (case), 10653160351436 (unit), Lot Numbers:   2022042050, 2022051680;   w) REF DYNDC2815A, UDI/DI 00653160348316 (case), 10653160348313 (unit), Lot  Numbers:  2022031450, 2022041180, 2022041280, 2022041380, 2022062080;   x) REF DT22270A, UDI/DI 00653160348255 (case), 10653160348252 (unit), Lot Numbers: 2022011350, 2022022880;    y) REF DM330A, UDI/DI 00653160324051 (case), 10653160324058 (unit), Lot Numbers:  2023081090, 2022042580, 2022103180, 2023020680, 2023042480;   z) REF DM330A, UDI/DI 00653160366655 (case), 10653160366652 (unit), Lot Numbers:  2023101190;   aa) REF DM875, UDI/DI 00653160309614 (case), 10653160309611 (unit), Lot Numbers:  2022040490;   bb) REF DM875, UDI/DI 00653160352504 (case), 10653160352501 (unit), Lot Numbers:  2022041290, 2022042590, 2022051990, 2022081990, 2022120990, 2023042790, 2023053090, 2023071490, 2023101290;   cc) REF DM1105, UDI/DI 00653160343519 (case), 10653160343516 (unit), Lot Numbers:  2022032490. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
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      "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-1136-2024&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-1136-2024&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-1136-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1136-2024 as Class I",
      "text": "The FDA assigned this recall Class I: Class I — the FDA judged there is a reasonable probability that use of the product would cause serious harm or death.. 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-1136-2024&lang=eng",
        "value": "Class I",
        "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-1136-2024&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-1136-2024/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": [
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      "name": "FDA recall details — Z-1136-2024",
      "numberOfItems": 9,
      "itemListElement": [
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1136-2024",
            "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 I",
            "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": "Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components):  0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.",
            "Status": "recorded"
          }
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          "@type": "schema:ListItem",
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          "item": {
            "Field": "Initiated",
            "Value": "2023-11-15",
            "Status": "recorded"
          }
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          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "a) REF DM405A, UDI/DI 00653160322217 (case), 10653160322214 (unit), Lot Numbers: 2022042580, 2022070580, 2022071180, 2022071880, 2022072580, 2022080180, 2023040380, 2023050180, 2023073180, 2023102380;    b) REF DM640, UDI/DI 00653160289602 (case), 10653160289609 (unit), Lot Numbers:  2022041390;   c) REF DM600, UDI/DI 00653160352610 (case), 10653160352617 (unit), Lot Numbers:  2022041880, 2023081480;   d) REF DM870A, UDI/DI 00653160348217 (case), 10653160348214 (unit), Lot Numbers: 2022020780;    e) REF DM870A, UDI/DI 00653160352382 (case), 10653160352389 (unit), Lot Numbers:   2022041880;   f) REF DT21465B, UDI/DI 00653160350005 (case), 10653160350002 (unit), Lot Numbers: 2022012550, 2022032880, 2022032980, 2022082280;    g) REF DT18905, UDI/DI 00653160275063 (case), 10653160275060 (unit), Lot Numbers:  2022040590, 2022041390, 2022081990, 2023011290, 2023012490, 2023051190, 2023061290, 2023081590, 2023101790;   h) REF DM610, UDI/DI 00653160294002 (case), 10653160294009 (unit), Lot Numbers:  2022050980, 2022072580, 2022072680, 2022080180, 2022080880, 2022081580, 2023050880, 2023061280, 2023072480, 2023081480, 2023082880;   i) REF DT18210, UDI/DI 00653160352658 (case), 10653160352655 (unit), Lot Numbers: 2022042290;    j) REF DT18695A, UDI/DI 00653160315127 (case), 10653160315124 (unit), Lot Numbers: 2022042790, 2022103190, 2023012790, 2023032490, 2023032890, 2023052690, 2023072890, 2023092190;   k) REF DM630, UDI/DI 00653160288568 (case), 10653160288565 (unit), Lot Numbers:  2022033190;   l) REF DM630, UDI/DI 00653160352450 (case), 10653160352457 (unit), Lot Numbers:  2022050590, 2022111790, 2023011990, 2023031590, 2023042490, 2023062690, 2023081490;   m) REF DT19005A, UDI/DI 00653160349801 (case), 10653160349808 (unit), Lot Numbers:   2022050980;     n) REF DM1060, UDI/DI 00653160352443 (case), 10653160352440 (unit), Lot Numbers:  2022050280, 2023070380, 2023082180, 2023082880, 2023101680;   o) REF DM525A, UDI/DI 00653160352511 (case), 10653160352518 (unit), Lot Numbers:  2022042580, 2022080180, 2022112880, 2022112980;   p) REF DM850, UDI/DI 00653160307047 (case), 10653160307044 (unit), Lot Numbers: 2022040490;    q) REF DT17355, UDI/DI 00653160265170 (case), 10653160265177 (unit), Lot Numbers:  2022082290, 2022090190, 2022112990, 2023012490, 2023042090, 2023070690, 2023073190, 2023081190;   r) REF DT19835B, UDI/DI 00653160350128 (case), 10653160350125 (unit), Lot Numbers:  2022021150, 2022022250;   s) REF DT22575A, UDI/DI 00653160349825 (case), 10653160349822 (unit), Lot Numbers: 2022011350, 2022052380, 2022052480, 2022052580;    t) REF DT20845B, UDI/DI 00653160348842 (case), 10653160348849 (unit), Lot Numbers: 2022010750, 2022031450;    u) REF DT20885B, UDI/DI 00653160348422 (case), 10653160348429 (unit), Lot Numbers:  2022052380;   v) REF DT21585B, UDI/DI 00653160351439 (case), 10653160351436 (unit), Lot Numbers:   2022042050, 2022051680;   w) REF DYNDC2815A, UDI/DI 00653160348316 (case), 10653160348313 (unit), Lot  Numbers:  2022031450, 2022041180, 2022041280, 2022041380, 2022062080;   x) REF DT22270A, UDI/DI 00653160348255 (case), 10653160348252 (unit), Lot Numbers: 2022011350, 2022022880;    y) REF DM330A, UDI/DI 00653160324051 (case), 10653160324058 (unit), Lot Numbers:  2023081090, 2022042580, 2022103180, 2023020680, 2023042480;   z) REF DM330A, UDI/DI 00653160366655 (case), 10653160366652 (unit), Lot Numbers:  2023101190;   aa) REF DM875, UDI/DI 00653160309614 (case), 10653160309611 (unit), Lot Numbers:  2022040490;   bb) REF DM875, UDI/DI 00653160352504 (case), 10653160352501 (unit), Lot Numbers:  2022041290, 2022042590, 2022051990, 2022081990, 2022120990, 2023042790, 2023053090, 2023071490, 2023101290;   cc) REF DM1105, UDI/DI 00653160343519 (case), 10653160343516 (unit), Lot Numbers:  2022032490",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}