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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0720-2025.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline brand, medical procedure convenience kits, labeled as: 1) SINUS CDS-1, SKU CDS982901F; 2) NASAL PACK, SKU DYNJ17493G; 3) FESS PACK-POB, SKU DYNJ33520A; 4) SINUS PACK, SKU DYNJ44845G; 5) SINUS PACK, SKU DYNJ48330B; 6) ENT PACK, SKU DYNJ50572; 7) ENT PACK, SKU DYNJ53573A; 8) ENT HUTCH, SKU DYNJ58856A; 9) PACK NASAL, SKU DYNJ60111A; 10) PACK NASAL, SKU DYNJ60111B; 11) ENT CUSTOM PACK, SKU DYNJ63052C; 12) ENT PACK, SKU DYNJ64256D; 13) FESS/SEPTOPLASTY PACK, SKU DYNJ64509B; 14) SINUS ENDOSCOPY PACK, SKU DYNJ65644; 15) ACOUSTICS SHSC-LF, SKU DYNJ66749; 16) TRANSPHENOIDAL PACK, SKU DYNJ67423A; 17) TRANSPHENOIDAL PACK, SKU DYNJ67423B; 18) ENT PACK, SKU DYNJ68102B; 19) E N T PACK, SKU DYNJ80526B; 20) NASAL PACK, SKU DYNJ81280; 21) ENT FESS PACK, SKU DYNJ81420A; 22) HEAD AND NECK PACK, SKU DYNJ81934; 23) HEAD AND NECK PACK - 51597, SKU DYNJ81934A; 24) HEAD AND NECK ENT PACK, SKU DYNJ83679A; 25) HEAD NECK PACK HC, SKU DYNJ84270; 26) TRANSPHENOIDAL PACK-LF, SKU DYNJ85422; 27) NASAL SEPTAL, SKU DYNJ901299A; 28) NASAL SEPTAL, SKU DYNJ901299B; 29) PACK TRANSPHENOIDAL, SKU DYNJ905685D; 30) SEPTOPLASTY, SKU DYNJ906474C; 31) LEFORTE MANDIBLE, SKU DYNJ906839A; 32) NASAL MHS, SKU DYNJ908545A; 33) NASAL MHS, SKU DYNJ908545B; 34) ENT, SKU DYNJ909128A; 35) ENT, SKU DYNJ909128C; 36) ENT, SKU DYNJ909128D; 37) ENT, SKU DYNJ909128F; 38) SINUS PACK, SKU DYNJ909370",
  "description": "FDA recall Z-0720-2025 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand, medical procedure convenience kits, labeled as: 1) SINUS CDS-1, SKU CDS982901F; 2) NASAL PACK, SKU DYNJ17493G; 3) FESS PACK-POB, SKU DYNJ33520A; 4) SINUS PACK, SKU DYNJ44845G; 5) SINUS PACK, SKU DYNJ48330B; 6) ENT PACK, SKU DYNJ50572; 7) ENT PACK, SKU DYNJ53573A; 8) ENT HUTCH, SKU DYNJ58856A; 9) PACK NASAL, SKU DYNJ60111A; 10) PACK NASAL, SKU DYNJ60111B; 11) ENT CUSTOM PACK, SKU DYNJ63052C; 12) ENT PACK, SKU DYNJ64256D; 13) FESS/SEPTOPLASTY PACK, SKU DYNJ64509B; 14) SINUS ENDOSCOPY PACK, SKU DYNJ65644; 15) ACOUSTICS SHSC-LF, SKU DYNJ66749; 16) TRANSPHENOIDAL PACK, SKU DYNJ67423A; 17) TRANSPHENOIDAL PACK, SKU DYNJ67423B; 18) ENT PACK, SKU DYNJ68102B; 19) E N T PACK, SKU DYNJ80526B; 20) NASAL PACK, SKU DYNJ81280; 21) ENT FESS PACK, SKU DYNJ81420A; 22) HEAD AND NECK PACK, SKU DYNJ81934; 23) HEAD AND NECK PACK - 51597, SKU DYNJ81934A; 24) HEAD AND NECK ENT PACK, SKU DYNJ83679A; 25) HEAD NECK PACK HC, SKU DYNJ84270; 26) TRANSPHENOIDAL PACK-LF, SKU DYNJ85422; 27) NASAL SEPTAL, SKU DYNJ901299A; 28) NASAL SEPTAL, SKU DYNJ901299B; 29) PACK TRANSPHENOIDAL, SKU DYNJ905685D; 30) SEPTOPLASTY, SKU DYNJ906474C; 31) LEFORTE MANDIBLE, SKU DYNJ906839A; 32) NASAL MHS, SKU DYNJ908545A; 33) NASAL MHS, SKU DYNJ908545B; 34) ENT, SKU DYNJ909128A; 35) ENT, SKU DYNJ909128C; 36) ENT, SKU DYNJ909128D; 37) ENT, SKU DYNJ909128F; 38) SINUS PACK, SKU DYNJ909370 (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,
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
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  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline brand, medical procedure convenience kits, labeled as: 1) SINUS CDS-1, SKU CDS982901F; 2) NASAL PACK, SKU DYNJ17493G; 3) FESS PACK-POB, SKU DYNJ33520A; 4) SINUS PACK, SKU DYNJ44845G; 5) SINUS PACK, SKU DYNJ48330B; 6) ENT PACK, SKU DYNJ50572; 7) ENT PACK, SKU DYNJ53573A; 8) ENT HUTCH, SKU DYNJ58856A; 9) PACK NASAL, SKU DYNJ60111A; 10) PACK NASAL, SKU DYNJ60111B; 11) ENT CUSTOM PACK, SKU DYNJ63052C; 12) ENT PACK, SKU DYNJ64256D; 13) FESS/SEPTOPLASTY PACK, SKU DYNJ64509B; 14) SINUS ENDOSCOPY PACK, SKU DYNJ65644; 15) ACOUSTICS SHSC-LF, SKU DYNJ66749; 16) TRANSPHENOIDAL PACK, SKU DYNJ67423A; 17) TRANSPHENOIDAL PACK, SKU DYNJ67423B; 18) ENT PACK, SKU DYNJ68102B; 19) E N T PACK, SKU DYNJ80526B; 20) NASAL PACK, SKU DYNJ81280; 21) ENT FESS PACK, SKU DYNJ81420A; 22) HEAD AND NECK PACK, SKU DYNJ81934; 23) HEAD AND NECK PACK - 51597, SKU DYNJ81934A; 24) HEAD AND NECK ENT PACK, SKU DYNJ83679A; 25) HEAD NECK PACK HC, SKU DYNJ84270; 26) TRANSPHENOIDAL PACK-LF, SKU DYNJ85422; 27) NASAL SEPTAL, SKU DYNJ901299A; 28) NASAL SEPTAL, SKU DYNJ901299B; 29) PACK TRANSPHENOIDAL, SKU DYNJ905685D; 30) SEPTOPLASTY, SKU DYNJ906474C; 31) LEFORTE MANDIBLE, SKU DYNJ906839A; 32) NASAL MHS, SKU DYNJ908545A; 33) NASAL MHS, SKU DYNJ908545B; 34) ENT, SKU DYNJ909128A; 35) ENT, SKU DYNJ909128C; 36) ENT, SKU DYNJ909128D; 37) ENT, SKU DYNJ909128F; 38) SINUS PACK, SKU DYNJ909370",
    "manufacturer": {
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      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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    {
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      "@type": "schema:Claim",
      "name": "FDA recall Z-0720-2025: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline brand, medical procedure convenience kits, labeled as: 1) SINUS CDS-1, SKU CDS982901F; 2) NASAL PACK, SKU DYNJ17493G; 3) FESS PACK-POB, SKU DYNJ33520A; 4) SINUS PACK, SKU DYNJ44845G; 5) SINUS PACK, SKU DYNJ48330B; 6) ENT PACK, SKU DYNJ50572; 7) ENT PACK, SKU DYNJ53573A; 8) ENT HUTCH, SKU DYNJ58856A; 9) PACK NASAL, SKU DYNJ60111A; 10) PACK NASAL, SKU DYNJ60111B; 11) ENT CUSTOM PACK, SKU DYNJ63052C; 12) ENT PACK, SKU DYNJ64256D; 13) FESS/SEPTOPLASTY PACK, SKU DYNJ64509B; 14) SINUS ENDOSCOPY PACK, SKU DYNJ65644; 15) ACOUSTICS SHSC-LF, SKU DYNJ66749; 16) TRANSPHENOIDAL PACK, SKU DYNJ67423A; 17) TRANSPHENOIDAL PACK, SKU DYNJ67423B; 18) ENT PACK, SKU DYNJ68102B; 19) E N T PACK, SKU DYNJ80526B; 20) NASAL PACK, SKU DYNJ81280; 21) ENT FESS PACK, SKU DYNJ81420A; 22) HEAD AND NECK PACK, SKU DYNJ81934; 23) HEAD AND NECK PACK - 51597, SKU DYNJ81934A; 24) HEAD AND NECK ENT PACK, SKU DYNJ83679A; 25) HEAD NECK PACK HC, SKU DYNJ84270; 26) TRANSPHENOIDAL PACK-LF, SKU DYNJ85422; 27) NASAL SEPTAL, SKU DYNJ901299A; 28) NASAL SEPTAL, SKU DYNJ901299B; 29) PACK TRANSPHENOIDAL, SKU DYNJ905685D; 30) SEPTOPLASTY, SKU DYNJ906474C; 31) LEFORTE MANDIBLE, SKU DYNJ906839A; 32) NASAL MHS, SKU DYNJ908545A; 33) NASAL MHS, SKU DYNJ908545B; 34) ENT, SKU DYNJ909128A; 35) ENT, SKU DYNJ909128C; 36) ENT, SKU DYNJ909128D; 37) ENT, SKU DYNJ909128F; 38) SINUS PACK, SKU DYNJ909370",
      "text": "The FDA logged enforcement record Z-0720-2025: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline brand, medical procedure convenience kits, labeled as: 1) SINUS CDS-1, SKU CDS982901F; 2) NASAL PACK, SKU DYNJ17493G; 3) FESS PACK-POB, SKU DYNJ33520A; 4) SINUS PACK, SKU DYNJ44845G; 5) SINUS PACK, SKU DYNJ48330B; 6) ENT PACK, SKU DYNJ50572; 7) ENT PACK, SKU DYNJ53573A; 8) ENT HUTCH, SKU DYNJ58856A; 9) PACK NASAL, SKU DYNJ60111A; 10) PACK NASAL, SKU DYNJ60111B; 11) ENT CUSTOM PACK, SKU DYNJ63052C; 12) ENT PACK, SKU DYNJ64256D; 13) FESS/SEPTOPLASTY PACK, SKU DYNJ64509B; 14) SINUS ENDOSCOPY PACK, SKU DYNJ65644; 15) ACOUSTICS SHSC-LF, SKU DYNJ66749; 16) TRANSPHENOIDAL PACK, SKU DYNJ67423A; 17) TRANSPHENOIDAL PACK, SKU DYNJ67423B; 18) ENT PACK, SKU DYNJ68102B; 19) E N T PACK, SKU DYNJ80526B; 20) NASAL PACK, SKU DYNJ81280; 21) ENT FESS PACK, SKU DYNJ81420A; 22) HEAD AND NECK PACK, SKU DYNJ81934; 23) HEAD AND NECK PACK - 51597, SKU DYNJ81934A; 24) HEAD AND NECK ENT PACK, SKU DYNJ83679A; 25) HEAD NECK PACK HC, SKU DYNJ84270; 26) TRANSPHENOIDAL PACK-LF, SKU DYNJ85422; 27) NASAL SEPTAL, SKU DYNJ901299A; 28) NASAL SEPTAL, SKU DYNJ901299B; 29) PACK TRANSPHENOIDAL, SKU DYNJ905685D; 30) SEPTOPLASTY, SKU DYNJ906474C; 31) LEFORTE MANDIBLE, SKU DYNJ906839A; 32) NASAL MHS, SKU DYNJ908545A; 33) NASAL MHS, SKU DYNJ908545B; 34) ENT, SKU DYNJ909128A; 35) ENT, SKU DYNJ909128C; 36) ENT, SKU DYNJ909128D; 37) ENT, SKU DYNJ909128F; 38) SINUS PACK, SKU DYNJ909370 — reason: Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods. Status: Ongoing — the recall is still being carried out.. Initiated 2024-11-06. Affected lots/codes: UDI-DI:  CDS982901F, 10889942216970 (each), 40889942216971 (case),  Lot Numbers: 23HBQ152;  UDI-DI:  DYNJ17493G, 10195327224424 (each), 40195327224425 (case),  Lot Numbers: 23GBW775;  UDI-DI:  DYNJ33520A, 10884389851333 (each), 40884389851334 (case),  Lot Numbers: 23HDB834;  UDI-DI:  DYNJ44845G, 10889942712311 (each), 40889942712312 (case),  Lot Numbers: 23HBF195;  UDI-DI:  DYNJ48330B, 10195327113506 (each), 40195327113507 (case),  Lot Numbers: 23HBO622;  UDI-DI:  DYNJ50572, 10889942008476 (each), 40889942008477 (case),  Lot Numbers: 23GBR940;  UDI-DI:  DYNJ53573A, 10193489201635 (each), 40193489201636 (case),  Lot Numbers: 23GBS356;  UDI-DI:  DYNJ58856A, 10193489750263 (each), 40193489750264 (case),  Lot Numbers: 23HBO870;  UDI-DI:  DYNJ60111A, 10193489246995 (each), 40193489246996 (case),  Lot Numbers: 21JMB783 21HMF433 21GMD178 21FMC923 20IMB575;  UDI-DI:  DYNJ60111B, 10195327527617 (each), 40195327527618 (case),  Lot Numbers: 24HMC974 24GMA899 24FMB079 24EMC108 24DMD791 24CMG320;  UDI-DI:  DYNJ63052C, 10195327101312 (each), 40195327101313 (case),  Lot Numbers: 22KME394 22KMA630 22JMD852 22GMG160 22EMG974 22DMF954 22CMC565;  UDI-DI:  DYNJ64256D, 10195327452773 (each), 40195327452774 (case),  Lot Numbers: 23HBA766;  UDI-DI:  DYNJ64509B, 10195327323745 (each), 40195327323746 (case),  Lot Numbers: 23HBC092;  UDI-DI:  DYNJ65644, 10193489283204 (each), 40193489283205 (case),  Lot Numbers: 23HBA753;  UDI-DI:  DYNJ66749, 10193489375947 (each), 40193489375948 (case),  Lot Numbers: 21ABT938 21ABO570 20JBS998 20HBM389;  UDI-DI:  DYNJ67423A, 10195327163402 (each), 40195327163403 (case),  Lot Numbers: 24DLA092 24BLA235 23KLA058 23ILB043 23ILA503 23HLB296 23HLB011 23FLA068 23DLA463 23DLA185 23BLA617 22LLA582 22KLA652 22HLA029 22GLA884;  UDI-DI:  DYNJ67423B, 10195327686871 (each), 40195327686872 (case),  Lot Numbers: 24GLB018 24FLA258 24ELA763 24DLA759;  UDI-DI:  DYNJ68102B, 10195327699369 (each), 40195327699360 (case),  Lot Numbers: 24IBB348 24GBB791 24EBA114;  UDI-DI:  DYNJ80526B, 10195327211059 (each), 40195327211050 (case),  Lot Numbers: 23HBF568;  UDI-DI:  DYNJ81280, 10195327102968 (each), 40195327102969 (case),  Lot Numbers: 22HMF910;  UDI-DI:  DYNJ81420A, 10195327322601 (each), 40195327322602 (case),  Lot Numbers: 24CBL416 23LBK136 23IBR308 23HBD265 23GBJ044 23FBK113 23EBN716 23BBQ143;  UDI-DI:  DYNJ81934, 10195327156817 (each), 40195327156818 (case),  Lot Numbers: 23EBG024 23BBC727 22JBJ632 22HBH399;  UDI-DI:  DYNJ81934A, 10195327413019 (each), 40195327413010 (case),  Lot Numbers: 24DBK564 24DBB486 24CBG998 24BBV700 24ABD320 23HBO084 23GBG012;  UDI-DI:  DYNJ83679A, 10195327459727 (each), 40195327459728 (case),  Lot Numbers: 24HBP441 24GBF665 24BBO428 23LBS373 23JBD663 23IBN314;  UDI-DI:  DYNJ84270, 10195327349103 (each), 40195327349104 (case),  Lot Numbers: 23GBC274;  UDI-DI:  DYNJ85422, 10195327499716 (each), 40195327499717 (case),  Lot Numbers: 24FDA925 24ADB100;  UDI-DI:  DYNJ901299A, 10889942010349 (each), 40889942010340 (case),  Lot Numbers: 21FBC250 20JBO761 20IBH831 20FBM501;  UDI-DI:  DYNJ901299B, 10193489923384 (each), 40193489923385 (case),  Lot Numbers: 22FBU440 22OBC118 22OBC120 22ABA377 21JBJ197 21IBM868 21GBO441;  UDI-DI:  DYNJ905685D, 10198459024139 (each), 40198459024130 (case),  Lot Numbers: 24IDB382;  UDI-DI:  DYNJ906474C, 10195327221355 (each), 40195327221356 (case),  Lot Numbers: 24HDA228 24EDA811 24DDB542 23LDB493 23GDA771 23DDA732 22IDB976;  UDI-DI:  DYNJ906839A, 10195327092528 (each), 40195327092529 (case),  Lot Numbers: 22JMB394;  UDI-DI:  DYNJ908545A, 10195327384166 (each), 40195327384167 (case),  Lot Numbers: 23JBV681;  UDI-DI:  DYNJ908545B, 10195327593124 (each), 40195327593125 (case),  Lot Numbers: 24HBI988 24FBS776 24FBA297 24ABT058;  UDI-DI:  DYNJ909128A, 10195327326739 (each), 40195327326730 (case),  Lot Numbers: 23EBD903 23DBD851;  UDI-DI:  DYNJ909128C, 10195327458416 (each), 40195327458417 (case),  Lot Numbers: 23JBO251 23HBI313;  UDI-DI:  DYNJ909128D, 10195327516321 (each), 40195327516322 (case),  Lot Numbers: 24EBC023 24CBK211 24BBM816 24ABR742 23LBQ695 23LBM416;  UDI-DI:  DYNJ909128F, 10198459055256 (each), 40198459055257 (case),  Lot Numbers: 24HBV054 24GBN495;  UDI-DI:  DYNJ909370, 10195327319038 (each), 40195327319039 (case),  Lot Numbers: 24BMA818 24AMG256 23LMF420 23LMB722 23LMA458 23CME287;. 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-0720-2025&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-0720-2025&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-0720-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0720-2025 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-0720-2025&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-0720-2025&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-0720-2025/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."
    }
  ],
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      "name": "FDA recall details — Z-0720-2025",
      "numberOfItems": 9,
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            "Field": "Recall number",
            "Value": "Z-0720-2025",
            "Status": "recorded"
          }
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        {
          "@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": "Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-11-06",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "UDI-DI:  CDS982901F, 10889942216970 (each), 40889942216971 (case),  Lot Numbers: 23HBQ152;  UDI-DI:  DYNJ17493G, 10195327224424 (each), 40195327224425 (case),  Lot Numbers: 23GBW775;  UDI-DI:  DYNJ33520A, 10884389851333 (each), 40884389851334 (case),  Lot Numbers: 23HDB834;  UDI-DI:  DYNJ44845G, 10889942712311 (each), 40889942712312 (case),  Lot Numbers: 23HBF195;  UDI-DI:  DYNJ48330B, 10195327113506 (each), 40195327113507 (case),  Lot Numbers: 23HBO622;  UDI-DI:  DYNJ50572, 10889942008476 (each), 40889942008477 (case),  Lot Numbers: 23GBR940;  UDI-DI:  DYNJ53573A, 10193489201635 (each), 40193489201636 (case),  Lot Numbers: 23GBS356;  UDI-DI:  DYNJ58856A, 10193489750263 (each), 40193489750264 (case),  Lot Numbers: 23HBO870;  UDI-DI:  DYNJ60111A, 10193489246995 (each), 40193489246996 (case),  Lot Numbers: 21JMB783 21HMF433 21GMD178 21FMC923 20IMB575;  UDI-DI:  DYNJ60111B, 10195327527617 (each), 40195327527618 (case),  Lot Numbers: 24HMC974 24GMA899 24FMB079 24EMC108 24DMD791 24CMG320;  UDI-DI:  DYNJ63052C, 10195327101312 (each), 40195327101313 (case),  Lot Numbers: 22KME394 22KMA630 22JMD852 22GMG160 22EMG974 22DMF954 22CMC565;  UDI-DI:  DYNJ64256D, 10195327452773 (each), 40195327452774 (case),  Lot Numbers: 23HBA766;  UDI-DI:  DYNJ64509B, 10195327323745 (each), 40195327323746 (case),  Lot Numbers: 23HBC092;  UDI-DI:  DYNJ65644, 10193489283204 (each), 40193489283205 (case),  Lot Numbers: 23HBA753;  UDI-DI:  DYNJ66749, 10193489375947 (each), 40193489375948 (case),  Lot Numbers: 21ABT938 21ABO570 20JBS998 20HBM389;  UDI-DI:  DYNJ67423A, 10195327163402 (each), 40195327163403 (case),  Lot Numbers: 24DLA092 24BLA235 23KLA058 23ILB043 23ILA503 23HLB296 23HLB011 23FLA068 23DLA463 23DLA185 23BLA617 22LLA582 22KLA652 22HLA029 22GLA884;  UDI-DI:  DYNJ67423B, 10195327686871 (each), 40195327686872 (case),  Lot Numbers: 24GLB018 24FLA258 24ELA763 24DLA759;  UDI-DI:  DYNJ68102B, 10195327699369 (each), 40195327699360 (case),  Lot Numbers: 24IBB348 24GBB791 24EBA114;  UDI-DI:  DYNJ80526B, 10195327211059 (each), 40195327211050 (case),  Lot Numbers: 23HBF568;  UDI-DI:  DYNJ81280, 10195327102968 (each), 40195327102969 (case),  Lot Numbers: 22HMF910;  UDI-DI:  DYNJ81420A, 10195327322601 (each), 40195327322602 (case),  Lot Numbers: 24CBL416 23LBK136 23IBR308 23HBD265 23GBJ044 23FBK113 23EBN716 23BBQ143;  UDI-DI:  DYNJ81934, 10195327156817 (each), 40195327156818 (case),  Lot Numbers: 23EBG024 23BBC727 22JBJ632 22HBH399;  UDI-DI:  DYNJ81934A, 10195327413019 (each), 40195327413010 (case),  Lot Numbers: 24DBK564 24DBB486 24CBG998 24BBV700 24ABD320 23HBO084 23GBG012;  UDI-DI:  DYNJ83679A, 10195327459727 (each), 40195327459728 (case),  Lot Numbers: 24HBP441 24GBF665 24BBO428 23LBS373 23JBD663 23IBN314;  UDI-DI:  DYNJ84270, 10195327349103 (each), 40195327349104 (case),  Lot Numbers: 23GBC274;  UDI-DI:  DYNJ85422, 10195327499716 (each), 40195327499717 (case),  Lot Numbers: 24FDA925 24ADB100;  UDI-DI:  DYNJ901299A, 10889942010349 (each), 40889942010340 (case),  Lot Numbers: 21FBC250 20JBO761 20IBH831 20FBM501;  UDI-DI:  DYNJ901299B, 10193489923384 (each), 40193489923385 (case),  Lot Numbers: 22FBU440 22OBC118 22OBC120 22ABA377 21JBJ197 21IBM868 21GBO441;  UDI-DI:  DYNJ905685D, 10198459024139 (each), 40198459024130 (case),  Lot Numbers: 24IDB382;  UDI-DI:  DYNJ906474C, 10195327221355 (each), 40195327221356 (case),  Lot Numbers: 24HDA228 24EDA811 24DDB542 23LDB493 23GDA771 23DDA732 22IDB976;  UDI-DI:  DYNJ906839A, 10195327092528 (each), 40195327092529 (case),  Lot Numbers: 22JMB394;  UDI-DI:  DYNJ908545A, 10195327384166 (each), 40195327384167 (case),  Lot Numbers: 23JBV681;  UDI-DI:  DYNJ908545B, 10195327593124 (each), 40195327593125 (case),  Lot Numbers: 24HBI988 24FBS776 24FBA297 24ABT058;  UDI-DI:  DYNJ909128A, 10195327326739 (each), 40195327326730 (case),  Lot Numbers: 23EBD903 23DBD851;  UDI-DI:  DYNJ909128C, 10195327458416 (each), 40195327458417 (case),  Lot Numbers: 23JBO251 23HBI313;  UDI-DI:  DYNJ909128D, 10195327516321 (each), 40195327516322 (case),  Lot Numbers: 24EBC023 24CBK211 24BBM816 24ABR742 23LBQ695 23LBM416;  UDI-DI:  DYNJ909128F, 10198459055256 (each), 40198459055257 (case),  Lot Numbers: 24HBV054 24GBN495;  UDI-DI:  DYNJ909370, 10195327319038 (each), 40195327319039 (case),  Lot Numbers: 24BMA818 24AMG256 23LMF420 23LMB722 23LMA458 23CME287;",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide. Canada.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}