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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1441-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "Centurion manual surgical kits labeled as:   a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225;   b) ST. KELLY HEMO W/TIPS (SK8039), Product Code 66565;   c) STERILE BUTTERFLY PROBE (P837), Product Code 66810;   d) STERILE PROBE (PR5), Product Code 66900;   e) STERILE NAIL NIPPER, Product Code 67110;   f) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code 67285;   g) STERILE 5 1/2\" NAIL NIPPER (32195), Product Code 67365;   h) STERILE 4 1/4\" CUTICLE NIPPER (32908), Product Code 67420;   i) STERILE ENGLISH ANVIL NAIL SPLITTER-5\", Product Code 67595;   j) STERILE UNIVERSAL RING CUTTER(FS02470), Product Code 67780;   k) STERILE FINGER NAIL CLIPPER, Product Code 589784ST;   l) BILLEAU EAR LOOP 4MM 6\" LARGE, Product Code BEL46ST;   m) PROBE WITH EYE, Product Code DYND04011;   n) STERILE 9\" MAYO SCISSOR (ST150), Product Code I67350;   o) STRL ROCHESTER OCHSNER SATIN 7 1/4\", Product Code I67695;   p) CMP* NAIL NIPPER ANGLED 4.5, Product Code I67980;   q) STERILE BILLEAU EAR LOOP 3MM, Product Code I67995;   r) ST. ALLIGATOR FORCEP, POINTED, MICRO P/S, Product Code I68020;   s) MOSQUITO HEMOSTAT FINE TIP, Product Code I68190;   t) STERILE VAS DEFERENS CLAMP (VDC100S), Product Code I68200;   u) LILLIE EAR HOOK, 7\" STERILE (P/S), Product Code I68305;   v) ST FOX DERMAL CURE, 4MM, 5 1/2  (32922), Product Code I68360;   w) STERILE SKIN HOOK - SHARP (SH25754), Product Code I68415;   x) ST. EYE LID SPECULUM WIRE ADULT (ES500P), Product Code I68460;   y) STERILE NAIL RASP DOUBLE ENDED (NR100), Product Code I68500;   z) ST. SCLERAL DEPRESSOR 5.5\" (SD500), Product Code I68515;   aa) STERILE NAIL SPLITTING FORCEP 4\" (NS400), Product Code I68600;   bb) STERILE 12\" PROBE W/ EYE, Product Code I68840;   cc) COMEDONE EXTRACTOR, STERILE (P/S), Product Code I86540;   dd) STERILE SPATULA & PACKER, Product Code I86695;   ee) STERILE - PHLBCTMY HOOK CRCHT STYL 6, Product Code I86875;   ff) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code P-67285    MEDLINE PROBE WITH EYE, Product Code DYND04011",
  "description": "FDA recall Z-1441-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling Centurion manual surgical kits labeled as:   a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225;   b) ST. KELLY HEMO W/TIPS (SK8039), Product Code 66565;   c) STERILE BUTTERFLY PROBE (P837), Product Code 66810;   d) STERILE PROBE (PR5), Product Code 66900;   e) STERILE NAIL NIPPER, Product Code 67110;   f) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code 67285;   g) STERILE 5 1/2\" NAIL NIPPER (32195), Product Code 67365;   h) STERILE 4 1/4\" CUTICLE NIPPER (32908), Product Code 67420;   i) STERILE ENGLISH ANVIL NAIL SPLITTER-5\", Product Code 67595;   j) STERILE UNIVERSAL RING CUTTER(FS02470), Product Code 67780;   k) STERILE FINGER NAIL CLIPPER, Product Code 589784ST;   l) BILLEAU EAR LOOP 4MM 6\" LARGE, Product Code BEL46ST;   m) PROBE WITH EYE, Product Code DYND04011;   n) STERILE 9\" MAYO SCISSOR (ST150), Product Code I67350;   o) STRL ROCHESTER OCHSNER SATIN 7 1/4\", Product Code I67695;   p) CMP* NAIL NIPPER ANGLED 4.5, Product Code I67980;   q) STERILE BILLEAU EAR LOOP 3MM, Product Code I67995;   r) ST. ALLIGATOR FORCEP, POINTED, MICRO P/S, Product Code I68020;   s) MOSQUITO HEMOSTAT FINE TIP, Product Code I68190;   t) STERILE VAS DEFERENS CLAMP (VDC100S), Product Code I68200;   u) LILLIE EAR HOOK, 7\" STERILE (P/S), Product Code I68305;   v) ST FOX DERMAL CURE, 4MM, 5 1/2  (32922), Product Code I68360;   w) STERILE SKIN HOOK - SHARP (SH25754), Product Code I68415;   x) ST. EYE LID SPECULUM WIRE ADULT (ES500P), Product Code I68460;   y) STERILE NAIL RASP DOUBLE ENDED (NR100), Product Code I68500;   z) ST. SCLERAL DEPRESSOR 5.5\" (SD500), Product Code I68515;   aa) STERILE NAIL SPLITTING FORCEP 4\" (NS400), Product Code I68600;   bb) STERILE 12\" PROBE W/ EYE, Product Code I68840;   cc) COMEDONE EXTRACTOR, STERILE (P/S), Product Code I86540;   dd) STERILE SPATULA & PACKER, Product Code I86695;   ee) STERILE - PHLBCTMY HOOK CRCHT STYL 6, Product Code I86875;   ff) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code P-67285    MEDLINE PROBE WITH EYE, Product Code DYND04011 (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.",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
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    "name": "openFDA drug & device enforcement (recall) reports",
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      "name": "U.S. Food & Drug Administration"
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1441-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Centurion manual surgical kits labeled as:   a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225;   b) ST. KELLY HEMO W/TIPS (SK8039), Product Code 66565;   c) STERILE BUTTERFLY PROBE (P837), Product Code 66810;   d) STERILE PROBE (PR5), Product Code 66900;   e) STERILE NAIL NIPPER, Product Code 67110;   f) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code 67285;   g) STERILE 5 1/2\" NAIL NIPPER (32195), Product Code 67365;   h) STERILE 4 1/4\" CUTICLE NIPPER (32908), Product Code 67420;   i) STERILE ENGLISH ANVIL NAIL SPLITTER-5\", Product Code 67595;   j) STERILE UNIVERSAL RING CUTTER(FS02470), Product Code 67780;   k) STERILE FINGER NAIL CLIPPER, Product Code 589784ST;   l) BILLEAU EAR LOOP 4MM 6\" LARGE, Product Code BEL46ST;   m) PROBE WITH EYE, Product Code DYND04011;   n) STERILE 9\" MAYO SCISSOR (ST150), Product Code I67350;   o) STRL ROCHESTER OCHSNER SATIN 7 1/4\", Product Code I67695;   p) CMP* NAIL NIPPER ANGLED 4.5, Product Code I67980;   q) STERILE BILLEAU EAR LOOP 3MM, Product Code I67995;   r) ST. ALLIGATOR FORCEP, POINTED, MICRO P/S, Product Code I68020;   s) MOSQUITO HEMOSTAT FINE TIP, Product Code I68190;   t) STERILE VAS DEFERENS CLAMP (VDC100S), Product Code I68200;   u) LILLIE EAR HOOK, 7\" STERILE (P/S), Product Code I68305;   v) ST FOX DERMAL CURE, 4MM, 5 1/2  (32922), Product Code I68360;   w) STERILE SKIN HOOK - SHARP (SH25754), Product Code I68415;   x) ST. EYE LID SPECULUM WIRE ADULT (ES500P), Product Code I68460;   y) STERILE NAIL RASP DOUBLE ENDED (NR100), Product Code I68500;   z) ST. SCLERAL DEPRESSOR 5.5\" (SD500), Product Code I68515;   aa) STERILE NAIL SPLITTING FORCEP 4\" (NS400), Product Code I68600;   bb) STERILE 12\" PROBE W/ EYE, Product Code I68840;   cc) COMEDONE EXTRACTOR, STERILE (P/S), Product Code I86540;   dd) STERILE SPATULA & PACKER, Product Code I86695;   ee) STERILE - PHLBCTMY HOOK CRCHT STYL 6, Product Code I86875;   ff) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code P-67285    MEDLINE PROBE WITH EYE, Product Code DYND04011",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
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  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1441-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1441-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling Centurion manual surgical kits labeled as:   a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225;   b) ST. KELLY HEMO W/TIPS (SK8039), Product Code 66565;   c) STERILE BUTTERFLY PROBE (P837), Product Code 66810;   d) STERILE PROBE (PR5), Product Code 66900;   e) STERILE NAIL NIPPER, Product Code 67110;   f) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code 67285;   g) STERILE 5 1/2\" NAIL NIPPER (32195), Product Code 67365;   h) STERILE 4 1/4\" CUTICLE NIPPER (32908), Product Code 67420;   i) STERILE ENGLISH ANVIL NAIL SPLITTER-5\", Product Code 67595;   j) STERILE UNIVERSAL RING CUTTER(FS02470), Product Code 67780;   k) STERILE FINGER NAIL CLIPPER, Product Code 589784ST;   l) BILLEAU EAR LOOP 4MM 6\" LARGE, Product Code BEL46ST;   m) PROBE WITH EYE, Product Code DYND04011;   n) STERILE 9\" MAYO SCISSOR (ST150), Product Code I67350;   o) STRL ROCHESTER OCHSNER SATIN 7 1/4\", Product Code I67695;   p) CMP* NAIL NIPPER ANGLED 4.5, Product Code I67980;   q) STERILE BILLEAU EAR LOOP 3MM, Product Code I67995;   r) ST. ALLIGATOR FORCEP, POINTED, MICRO P/S, Product Code I68020;   s) MOSQUITO HEMOSTAT FINE TIP, Product Code I68190;   t) STERILE VAS DEFERENS CLAMP (VDC100S), Product Code I68200;   u) LILLIE EAR HOOK, 7\" STERILE (P/S), Product Code I68305;   v) ST FOX DERMAL CURE, 4MM, 5 1/2  (32922), Product Code I68360;   w) STERILE SKIN HOOK - SHARP (SH25754), Product Code I68415;   x) ST. EYE LID SPECULUM WIRE ADULT (ES500P), Product Code I68460;   y) STERILE NAIL RASP DOUBLE ENDED (NR100), Product Code I68500;   z) ST. SCLERAL DEPRESSOR 5.5\" (SD500), Product Code I68515;   aa) STERILE NAIL SPLITTING FORCEP 4\" (NS400), Product Code I68600;   bb) STERILE 12\" PROBE W/ EYE, Product Code I68840;   cc) COMEDONE EXTRACTOR, STERILE (P/S), Product Code I86540;   dd) STERILE SPATULA & PACKER, Product Code I86695;   ee) STERILE - PHLBCTMY HOOK CRCHT STYL 6, Product Code I86875;   ff) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code P-67285    MEDLINE PROBE WITH EYE, Product Code DYND04011",
      "text": "The FDA logged enforcement record Z-1441-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Centurion manual surgical kits labeled as:   a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225;   b) ST. KELLY HEMO W/TIPS (SK8039), Product Code 66565;   c) STERILE BUTTERFLY PROBE (P837), Product Code 66810;   d) STERILE PROBE (PR5), Product Code 66900;   e) STERILE NAIL NIPPER, Product Code 67110;   f) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code 67285;   g) STERILE 5 1/2\" NAIL NIPPER (32195), Product Code 67365;   h) STERILE 4 1/4\" CUTICLE NIPPER (32908), Product Code 67420;   i) STERILE ENGLISH ANVIL NAIL SPLITTER-5\", Product Code 67595;   j) STERILE UNIVERSAL RING CUTTER(FS02470), Product Code 67780;   k) STERILE FINGER NAIL CLIPPER, Product Code 589784ST;   l) BILLEAU EAR LOOP 4MM 6\" LARGE, Product Code BEL46ST;   m) PROBE WITH EYE, Product Code DYND04011;   n) STERILE 9\" MAYO SCISSOR (ST150), Product Code I67350;   o) STRL ROCHESTER OCHSNER SATIN 7 1/4\", Product Code I67695;   p) CMP* NAIL NIPPER ANGLED 4.5, Product Code I67980;   q) STERILE BILLEAU EAR LOOP 3MM, Product Code I67995;   r) ST. ALLIGATOR FORCEP, POINTED, MICRO P/S, Product Code I68020;   s) MOSQUITO HEMOSTAT FINE TIP, Product Code I68190;   t) STERILE VAS DEFERENS CLAMP (VDC100S), Product Code I68200;   u) LILLIE EAR HOOK, 7\" STERILE (P/S), Product Code I68305;   v) ST FOX DERMAL CURE, 4MM, 5 1/2  (32922), Product Code I68360;   w) STERILE SKIN HOOK - SHARP (SH25754), Product Code I68415;   x) ST. EYE LID SPECULUM WIRE ADULT (ES500P), Product Code I68460;   y) STERILE NAIL RASP DOUBLE ENDED (NR100), Product Code I68500;   z) ST. SCLERAL DEPRESSOR 5.5\" (SD500), Product Code I68515;   aa) STERILE NAIL SPLITTING FORCEP 4\" (NS400), Product Code I68600;   bb) STERILE 12\" PROBE W/ EYE, Product Code I68840;   cc) COMEDONE EXTRACTOR, STERILE (P/S), Product Code I86540;   dd) STERILE SPATULA & PACKER, Product Code I86695;   ee) STERILE - PHLBCTMY HOOK CRCHT STYL 6, Product Code I86875;   ff) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code P-67285    MEDLINE PROBE WITH EYE, Product Code DYND04011 — reason: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-02-23. Affected lots/codes: a) 66225, UDI/DI 60653160018327 (case) 00653160018325 (each), Lot Numbers:  2023070390;   b) 66565, UDI/DI 20653160059865 (case) 00653160059861 (each), Lot Numbers:  2023022090;   c) 66810, UDI/DI 60653160038547 (case) 00653160038545 (each), Lot Numbers:  2023042490;   d) 66900, UDI/DI 60653160038868 (case) 00653160038866 (each), Lot Numbers:  2023030890, 2023100390, 2023111090;   e) 67110, UDI/DI 50653160049751 (case) 00653160049756 (each), Lot Numbers:  2023042490, 2023051590, 2023110290;   f) 67285, UDI/DI 50653160089139 (case) 00653160089134 (each), Lot Numbers:  2023081490, 2023101190;   g) 67365, UDI/DI 10653160115120 (case) 00653160115123 (each), Lot Numbers:  2023040390, 2023090790, 2023101790, 2023110890;   h) 67420, UDI/DI 10653160123491 (case) 00653160123494 (each), Lot Numbers:  2023100590;   i) 67595, UDI/DI 10653160184553 (case) 00653160184556 (each), Lot Numbers:  2023032890, 2023101390;   j) 67780, UDI/DI 10653160196662 (case) 00653160196665 (each), Lot Numbers:  2023071290;   k) 589784ST, UDI/DI 40653160130681 (case) 00653160130683 (each), Lot Numbers:  2023020990, 2023030790, 2023042890;   l) BEL46ST, UDI/DI 10653160227168 (case) 00653160227161 (each), Lot Numbers:  2023101890;   m) DYND04011, UDI/DI 40884389097800 (case) 10884389097809 (each), Lot Numbers:  2023102090;   n) I67350, UDI/DI 00653160286847 (case) 10653160286844 (each), Lot Numbers:  2023031390, 2023111790;   o) I67695, UDI/DI 00653160263060 (case) 10653160263067 (each), Lot Numbers:  2023110290 (not distributed);   p) I67980, UDI/DI 10653160224815 (case) 00653160224818 (each), Lot Numbers:  2023031690;   q) I67995, UDI/DI 10653160227656 (case) 00653160227659 (each), Lot Numbers:  2023042690, 2023101790, 2023111090;   r) I68020, UDI/DI 10653160228349 (case) 00653160228342 (each), Lot Numbers:  2023092990, 2023111590;   s) I68190, UDI/DI 00653160263299 (case) 10653160263296 (each), Lot Numbers:  2023041390, 2023090790;   t) I68200, UDI/DI 00653160263077 (case) 10653160263074 (each), Lot Numbers:  2023101890;   u) I68305, UDI/DI 00653160277647 (case) 10653160277644 (each), Lot Numbers:  2023072090;   v) I68360, UDI/DI 00653160280852 (case) 10653160280859 (each), Lot Numbers:  2023021490;   w) I68415, UDI/DI 00653160286946 (case) 10653160286943 (each), Lot Numbers:  2023111790;   x) I68460, UDI/DI 00653160289886 (case) 10653160289883 (each), Lot Numbers:  2023030990, 2023060690, 2023100390;   y) I68500, UDI/DI 00653160293555 (case) 10653160293552 (each), Lot Numbers:  2023061490, 2023111390;   z) I68515, UDI/DI 00653160293548 (case) 10653160293545 (each), Lot Numbers:  2023061290;   aa) I68600, UDI/DI 00653160308334 (case) 10653160308331 (each), Lot Numbers:  2023042790;   bb) I68840, UDI/DI 00653160331578 (case) 10653160331575 (each), Lot Numbers:  2023021690, 2023050890, 2023091890;   cc) I86540, UDI/DI 00653160270907 (case) 10653160270904 (each), Lot Numbers:  2023041390;   dd) I86695, UDI/DI 00653160291834 (case) 10653160291831 (each), Lot Numbers:  2023042090;   ee) I86875, UDI/DI 00653160359190 (case) 10653160359197 (each), Lot Numbers:  2023032790;   ff) P-67285, UDI/DI 50653160089139 (case) 00653160089134 (each), Lot Numbers:  2023120590  MEDLINE: UDI/DI 40884389097800  (case), 10884389097809 (each), Lot Numbers:  2023102090. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": true,
        "supported": true,
        "adjudged": true,
        "operative": true
      },
      "grounding": {
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        "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-1441-2024&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-1441-2024&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-1441-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1441-2024 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-1441-2024&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-1441-2024&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-1441-2024/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-1441-2024",
      "numberOfItems": 9,
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-1441-2024",
            "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 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": "Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-02-23",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "a) 66225, UDI/DI 60653160018327 (case) 00653160018325 (each), Lot Numbers:  2023070390;   b) 66565, UDI/DI 20653160059865 (case) 00653160059861 (each), Lot Numbers:  2023022090;   c) 66810, UDI/DI 60653160038547 (case) 00653160038545 (each), Lot Numbers:  2023042490;   d) 66900, UDI/DI 60653160038868 (case) 00653160038866 (each), Lot Numbers:  2023030890, 2023100390, 2023111090;   e) 67110, UDI/DI 50653160049751 (case) 00653160049756 (each), Lot Numbers:  2023042490, 2023051590, 2023110290;   f) 67285, UDI/DI 50653160089139 (case) 00653160089134 (each), Lot Numbers:  2023081490, 2023101190;   g) 67365, UDI/DI 10653160115120 (case) 00653160115123 (each), Lot Numbers:  2023040390, 2023090790, 2023101790, 2023110890;   h) 67420, UDI/DI 10653160123491 (case) 00653160123494 (each), Lot Numbers:  2023100590;   i) 67595, UDI/DI 10653160184553 (case) 00653160184556 (each), Lot Numbers:  2023032890, 2023101390;   j) 67780, UDI/DI 10653160196662 (case) 00653160196665 (each), Lot Numbers:  2023071290;   k) 589784ST, UDI/DI 40653160130681 (case) 00653160130683 (each), Lot Numbers:  2023020990, 2023030790, 2023042890;   l) BEL46ST, UDI/DI 10653160227168 (case) 00653160227161 (each), Lot Numbers:  2023101890;   m) DYND04011, UDI/DI 40884389097800 (case) 10884389097809 (each), Lot Numbers:  2023102090;   n) I67350, UDI/DI 00653160286847 (case) 10653160286844 (each), Lot Numbers:  2023031390, 2023111790;   o) I67695, UDI/DI 00653160263060 (case) 10653160263067 (each), Lot Numbers:  2023110290 (not distributed);   p) I67980, UDI/DI 10653160224815 (case) 00653160224818 (each), Lot Numbers:  2023031690;   q) I67995, UDI/DI 10653160227656 (case) 00653160227659 (each), Lot Numbers:  2023042690, 2023101790, 2023111090;   r) I68020, UDI/DI 10653160228349 (case) 00653160228342 (each), Lot Numbers:  2023092990, 2023111590;   s) I68190, UDI/DI 00653160263299 (case) 10653160263296 (each), Lot Numbers:  2023041390, 2023090790;   t) I68200, UDI/DI 00653160263077 (case) 10653160263074 (each), Lot Numbers:  2023101890;   u) I68305, UDI/DI 00653160277647 (case) 10653160277644 (each), Lot Numbers:  2023072090;   v) I68360, UDI/DI 00653160280852 (case) 10653160280859 (each), Lot Numbers:  2023021490;   w) I68415, UDI/DI 00653160286946 (case) 10653160286943 (each), Lot Numbers:  2023111790;   x) I68460, UDI/DI 00653160289886 (case) 10653160289883 (each), Lot Numbers:  2023030990, 2023060690, 2023100390;   y) I68500, UDI/DI 00653160293555 (case) 10653160293552 (each), Lot Numbers:  2023061490, 2023111390;   z) I68515, UDI/DI 00653160293548 (case) 10653160293545 (each), Lot Numbers:  2023061290;   aa) I68600, UDI/DI 00653160308334 (case) 10653160308331 (each), Lot Numbers:  2023042790;   bb) I68840, UDI/DI 00653160331578 (case) 10653160331575 (each), Lot Numbers:  2023021690, 2023050890, 2023091890;   cc) I86540, UDI/DI 00653160270907 (case) 10653160270904 (each), Lot Numbers:  2023041390;   dd) I86695, UDI/DI 00653160291834 (case) 10653160291831 (each), Lot Numbers:  2023042090;   ee) I86875, UDI/DI 00653160359190 (case) 10653160359197 (each), Lot Numbers:  2023032790;   ff) P-67285, UDI/DI 50653160089139 (case) 00653160089134 (each), Lot Numbers:  2023120590  MEDLINE: UDI/DI 40884389097800  (case), 10884389097809 (each), Lot Numbers:  2023102090",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Worldwide distribution - US Nationwide and the countries of Panama, Canada.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}