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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2714-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "Medline medical procedure kits labeled as follows:    a) ARTHROSCOPY, REF DYNJ909699;   b) BACK CDS, REF CDS984000C;   c) EXTREMITY, REF DYNJ900847A;   d) HAND-LF, REF DYNJ902619G;   e) HIP PINNING CDS, REF CDS984009C;   f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K;   g) KNEE, REF DYNJ904771B;   h) KNEE ARTHROSCOPY, REF DYNJ905519D;   i) KNEE ARTHROSCOPY, REF DYNJ906273F;   j) KNEE ARTHROSCOPY, REF DYNJ909747;   k) KNEE ARTHROSCOPY V, REF DYNJS2029D;   l) LAMINECTOMY, REF DYNJ907159A;   m) LOWER EXTREMITY, REF DYNJ904767A;   n) LOWER EXTREMITY, REF DYNJ905518F;   o) LOWER EXTREMITY, REF DYNJ909938;   p) MINOR EXTREMITY, REF DYNJ909939;   q) PODIATRY, REF DYNJ906275D;   r) SHOULDER, REF DYNJ904769C;   s) SHOULDER, REF DYNJ905511D;   t) SHOULDER, REF DYNJ909749;   u) SHOULDER ARTHROSCOPY, REF DYNJ906274F;   v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C;   w) SOUTH EXTREMITY, REF DYNJ909212A;   x) SPINE, REF DYNJ905512F;   y) TOTAL, REF DYNJ909704;   z) TOTAL HIP, REF DYNJ907157A;   aa) TOTAL HIP BASIC, REF DYNJ902368K;   bb) TOTAL JOINT, REF DYNJ905513G;   cc) TOTAL JOINT, REF DYNJ908375C;   dd) TOTAL JOINT II, REF DYNJS2027F;   ee) TOTAL KNEE, REF DYNJ907158A;   ff) TOTAL KNEE CDS, REF CDS983991C;   gg) TOTAL SHOULDER, REF DYNJ902367J;   hh) TURK-HAND, REF DYNJ905852C;   ii) UPPER EXTREMITY, REF DYNJ905514D",
  "description": "FDA recall Z-2714-2024 — MEDLINE INDUSTRIES, LP - Northfield is recalling Medline medical procedure kits labeled as follows:    a) ARTHROSCOPY, REF DYNJ909699;   b) BACK CDS, REF CDS984000C;   c) EXTREMITY, REF DYNJ900847A;   d) HAND-LF, REF DYNJ902619G;   e) HIP PINNING CDS, REF CDS984009C;   f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K;   g) KNEE, REF DYNJ904771B;   h) KNEE ARTHROSCOPY, REF DYNJ905519D;   i) KNEE ARTHROSCOPY, REF DYNJ906273F;   j) KNEE ARTHROSCOPY, REF DYNJ909747;   k) KNEE ARTHROSCOPY V, REF DYNJS2029D;   l) LAMINECTOMY, REF DYNJ907159A;   m) LOWER EXTREMITY, REF DYNJ904767A;   n) LOWER EXTREMITY, REF DYNJ905518F;   o) LOWER EXTREMITY, REF DYNJ909938;   p) MINOR EXTREMITY, REF DYNJ909939;   q) PODIATRY, REF DYNJ906275D;   r) SHOULDER, REF DYNJ904769C;   s) SHOULDER, REF DYNJ905511D;   t) SHOULDER, REF DYNJ909749;   u) SHOULDER ARTHROSCOPY, REF DYNJ906274F;   v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C;   w) SOUTH EXTREMITY, REF DYNJ909212A;   x) SPINE, REF DYNJ905512F;   y) TOTAL, REF DYNJ909704;   z) TOTAL HIP, REF DYNJ907157A;   aa) TOTAL HIP BASIC, REF DYNJ902368K;   bb) TOTAL JOINT, REF DYNJ905513G;   cc) TOTAL JOINT, REF DYNJ908375C;   dd) TOTAL JOINT II, REF DYNJS2027F;   ee) TOTAL KNEE, REF DYNJ907158A;   ff) TOTAL KNEE CDS, REF CDS983991C;   gg) TOTAL SHOULDER, REF DYNJ902367J;   hh) TURK-HAND, REF DYNJ905852C;   ii) UPPER EXTREMITY, REF DYNJ905514D (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/",
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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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    "creator": {
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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-2714-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medline medical procedure kits labeled as follows:    a) ARTHROSCOPY, REF DYNJ909699;   b) BACK CDS, REF CDS984000C;   c) EXTREMITY, REF DYNJ900847A;   d) HAND-LF, REF DYNJ902619G;   e) HIP PINNING CDS, REF CDS984009C;   f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K;   g) KNEE, REF DYNJ904771B;   h) KNEE ARTHROSCOPY, REF DYNJ905519D;   i) KNEE ARTHROSCOPY, REF DYNJ906273F;   j) KNEE ARTHROSCOPY, REF DYNJ909747;   k) KNEE ARTHROSCOPY V, REF DYNJS2029D;   l) LAMINECTOMY, REF DYNJ907159A;   m) LOWER EXTREMITY, REF DYNJ904767A;   n) LOWER EXTREMITY, REF DYNJ905518F;   o) LOWER EXTREMITY, REF DYNJ909938;   p) MINOR EXTREMITY, REF DYNJ909939;   q) PODIATRY, REF DYNJ906275D;   r) SHOULDER, REF DYNJ904769C;   s) SHOULDER, REF DYNJ905511D;   t) SHOULDER, REF DYNJ909749;   u) SHOULDER ARTHROSCOPY, REF DYNJ906274F;   v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C;   w) SOUTH EXTREMITY, REF DYNJ909212A;   x) SPINE, REF DYNJ905512F;   y) TOTAL, REF DYNJ909704;   z) TOTAL HIP, REF DYNJ907157A;   aa) TOTAL HIP BASIC, REF DYNJ902368K;   bb) TOTAL JOINT, REF DYNJ905513G;   cc) TOTAL JOINT, REF DYNJ908375C;   dd) TOTAL JOINT II, REF DYNJS2027F;   ee) TOTAL KNEE, REF DYNJ907158A;   ff) TOTAL KNEE CDS, REF CDS983991C;   gg) TOTAL SHOULDER, REF DYNJ902367J;   hh) TURK-HAND, REF DYNJ905852C;   ii) UPPER EXTREMITY, REF DYNJ905514D",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "MEDLINE INDUSTRIES, LP - Northfield"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-2714-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-2714-2024: MEDLINE INDUSTRIES, LP - Northfield is recalling Medline medical procedure kits labeled as follows:    a) ARTHROSCOPY, REF DYNJ909699;   b) BACK CDS, REF CDS984000C;   c) EXTREMITY, REF DYNJ900847A;   d) HAND-LF, REF DYNJ902619G;   e) HIP PINNING CDS, REF CDS984009C;   f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K;   g) KNEE, REF DYNJ904771B;   h) KNEE ARTHROSCOPY, REF DYNJ905519D;   i) KNEE ARTHROSCOPY, REF DYNJ906273F;   j) KNEE ARTHROSCOPY, REF DYNJ909747;   k) KNEE ARTHROSCOPY V, REF DYNJS2029D;   l) LAMINECTOMY, REF DYNJ907159A;   m) LOWER EXTREMITY, REF DYNJ904767A;   n) LOWER EXTREMITY, REF DYNJ905518F;   o) LOWER EXTREMITY, REF DYNJ909938;   p) MINOR EXTREMITY, REF DYNJ909939;   q) PODIATRY, REF DYNJ906275D;   r) SHOULDER, REF DYNJ904769C;   s) SHOULDER, REF DYNJ905511D;   t) SHOULDER, REF DYNJ909749;   u) SHOULDER ARTHROSCOPY, REF DYNJ906274F;   v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C;   w) SOUTH EXTREMITY, REF DYNJ909212A;   x) SPINE, REF DYNJ905512F;   y) TOTAL, REF DYNJ909704;   z) TOTAL HIP, REF DYNJ907157A;   aa) TOTAL HIP BASIC, REF DYNJ902368K;   bb) TOTAL JOINT, REF DYNJ905513G;   cc) TOTAL JOINT, REF DYNJ908375C;   dd) TOTAL JOINT II, REF DYNJS2027F;   ee) TOTAL KNEE, REF DYNJ907158A;   ff) TOTAL KNEE CDS, REF CDS983991C;   gg) TOTAL SHOULDER, REF DYNJ902367J;   hh) TURK-HAND, REF DYNJ905852C;   ii) UPPER EXTREMITY, REF DYNJ905514D",
      "text": "The FDA logged enforcement record Z-2714-2024: MEDLINE INDUSTRIES, LP - Northfield is voluntarily recalling Medline medical procedure kits labeled as follows:    a) ARTHROSCOPY, REF DYNJ909699;   b) BACK CDS, REF CDS984000C;   c) EXTREMITY, REF DYNJ900847A;   d) HAND-LF, REF DYNJ902619G;   e) HIP PINNING CDS, REF CDS984009C;   f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K;   g) KNEE, REF DYNJ904771B;   h) KNEE ARTHROSCOPY, REF DYNJ905519D;   i) KNEE ARTHROSCOPY, REF DYNJ906273F;   j) KNEE ARTHROSCOPY, REF DYNJ909747;   k) KNEE ARTHROSCOPY V, REF DYNJS2029D;   l) LAMINECTOMY, REF DYNJ907159A;   m) LOWER EXTREMITY, REF DYNJ904767A;   n) LOWER EXTREMITY, REF DYNJ905518F;   o) LOWER EXTREMITY, REF DYNJ909938;   p) MINOR EXTREMITY, REF DYNJ909939;   q) PODIATRY, REF DYNJ906275D;   r) SHOULDER, REF DYNJ904769C;   s) SHOULDER, REF DYNJ905511D;   t) SHOULDER, REF DYNJ909749;   u) SHOULDER ARTHROSCOPY, REF DYNJ906274F;   v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C;   w) SOUTH EXTREMITY, REF DYNJ909212A;   x) SPINE, REF DYNJ905512F;   y) TOTAL, REF DYNJ909704;   z) TOTAL HIP, REF DYNJ907157A;   aa) TOTAL HIP BASIC, REF DYNJ902368K;   bb) TOTAL JOINT, REF DYNJ905513G;   cc) TOTAL JOINT, REF DYNJ908375C;   dd) TOTAL JOINT II, REF DYNJS2027F;   ee) TOTAL KNEE, REF DYNJ907158A;   ff) TOTAL KNEE CDS, REF CDS983991C;   gg) TOTAL SHOULDER, REF DYNJ902367J;   hh) TURK-HAND, REF DYNJ905852C;   ii) UPPER EXTREMITY, REF DYNJ905514D — reason: A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-03-22. Affected lots/codes: a) REF DYNJ909699, UDI/DI 40195327446759 (case), 10195327446758 (unit), Lot Numbers:  DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699;   b) REF CDS984000C, UDI/DI 40889942011552 (case), 10889942011551 (unit), Lot Numbers:  22GBT604, 22IBI040, 23ABA955, 23DBT170, 23EBU747, 23HBB409;   c) REF DYNJ900847A, UDI/DI 40888277771209 (case), 10888277771208 (unit), Lot Numbers:    d) REF DYNJ902619G, UDI/DI 40195327214488 (case), 10195327214487 (unit), Lot Numbers:  22FBG650, 22FBK152, 22FBW287, 22HBA416, 22HBG372, 22HBS529, 22JBA184, 23EBC466, 23HBL953;   e) REF CDS984009C, UDI/DI 40888277768971 (case), 10888277768970 (unit), Lot Numbers:  22FBL426, 22GBU282, 23CBD236, 23HBY917;   f) REF DYNJ902380K, UDI/DI 40195327507009 (case), 10195327507008 (unit), Lot Numbers:  23KBX257;   g) REF DYNJ904771B, UDI/DI 40195327137190 (case), 10195327137199 (unit), Lot Numbers:  22EMB001, 22IMF542, 22KMC063, 23AME421, 23CMC716, 23DME033, 23FMI125, 23HMC273, 23HMI602, 23LME735;   h) REF DYNJ905519D, UDI/DI 40193489967396 (case), 10193489967395 (unit), Lot Numbers:  22GMG221, 22HMB217, 22LMJ233, 23AME962, 23AMI318, 23AMJ640, 23DMI673, 23IMG465, 23LMD163;   i) REF DYNJ906273F, UDI/DI 40195327511013 (case), 10195327511012 (unit), Lot Numbers:  23JBH985;   j) REF DYNJ909747, UDI/DI 40195327468201 (case), 10195327468200 (unit), Lot Numbers: 23HBZ535, 23KBF559;   k) REF DYNJS2029D, UDI/DI 40193489214414 (case), 10193489214413 (unit), Lot Numbers:  22IDA884, 22LDA526, 23CDA885, 23FDA459, 23JDB741;   l) REF DYNJ907159A, UDI/DI 40193489970419 (case), 10193489970418 (unit), Lot Numbers:  22EME489, 22FMH850, 22IMA282, 22JME894, 22LME340, 23AMB899, 23AMB937, 23AMF082, 23AMG074, 23AMJ063, 23BMF089, 23CMA038, 23FMF222, 23GMB990, 23GMF747, 23HMH495, 23JMC384, 23LMD528;   m) REF DYNJ904767A, UDI/DI 40889942850953 (case), 10889942850952 (unit), Lot Numbers:  22EMI503, 22IMC879, 22KMD093, 22LME746, 23AMC120, 23DMA417, 23DMD168, 23FME590, 23GMH321, 23HMG168;   n) REF DYNJ905518F, UDI/DI 40195327040407 (case), 10195327040406 (unit), Lot Numbers:  22FMI412, 22HMD694, 22IMA909, 22JMC316, 22KMC860, 22LMD325, 23AMF318, 23BMG871, 23EMF948, 23FMA357, 23GMD311, 23HMG163, 23JMA417, 23KMB755, 23LME256;   o) REF DYNJ909938, UDI/DI 40195327511228 (case), 10195327511227 (unit), Lot Numbers:  23JBI008;   p) REF DYNJ909939, UDI/DI 40195327511235 (case), 10195327511234 (unit), Lot Numbers:  23JBH778, 23KBU569;   q) REF DYNJ906275D, UDI/DI 40195327510986 (case), 10195327510985 (unit), Lot Numbers:  23JBI291, 23LBO829;   r) REF DYNJ904769C, UDI/DI 40195327137039 (case), 10195327137038 (unit), Lot Numbers:  22FMB469, 22IMA132, 22KMD488, 22LME616, 23GMF950, 23HME593, 23JMG901, 23KMG320;   s) REF DYNJ905511D, UDI/DI 40193489967549 (case), 10193489967548 (unit), Lot Numbers:  DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D;   t) REF DYNJ909749, UDI/DI 40195327468225 (case), 10195327468224 (unit), Lot Numbers:  23IBM342;   u) REF DYNJ906274F, UDI/DI 40195327511020 (case), 10195327511029 (unit), Lot Numbers:  23JBQ500, 23LBI456;   v) REF CDS984008C, UDI/DI 40888277768988 (case), 10888277768987 (unit), Lot Numbers:  22GBL020, 22JBE903, 23ABI396, 23ABM540, 23CBO804;   w) REF DYNJ909212A, UDI/DI 40195327493241 (case), 10195327493240 (unit), Lot Numbers:  23JBA160, 23KBA970;   x) REF DYNJ905512F, UDI/DI 40195327225378 (case), 10195327225377 (unit), Lot Numbers:  22JME529, 22KMD611, 22LMI893, 23BMI268, 23CMF328, 23FMG242, 23HMH500, 23IMC073, 23IMG464, 23JMI252, 23LMC546;   y) REF DYNJ909704, UDI/DI 40195327446919 (case), 10195327446918 (unit), Lot Numbers:  23GBN059, 23KBA374;   z) REF DYNJ907157A, UDI/DI 40193489970358 (case), 10193489970357 (unit), Lot Numbers:  22FMD804, 22JMG489, 22LMC517, 23BMA251, 23CMC137, 23CME146, 23DMA129, 23EMF952, 23FMG076, 23GMI555, 23IME182, 23JMI348, 23KMA447;   aa) REF DYNJ902368K, UDI/DI 40195327505890 (case), 10195327505899 (unit), Lot Numbers:  23JBI661, 23KBT583;   bb) REF DYNJ905513G, UDI/DI 40193489968027 (case), 10193489968026 (unit), Lot Numbers:  22FMG260, 22JMB517, 22JMF062, 23BME809, 23BMF391, 23BMG366, 23BMG367, 23BMI412, 23EMB428, 23FMA677, 23GMD648, 23JMC096, 23KMB846, 23LMC515;   cc) REF DYNJ908375C, UDI/DI 40195327484263 (case), 10195327484262 (unit), Lot Numbers:  23IBL834, 23KBD095, 23LBB392;   dd) REF DYNJS2027F, UDI/DI 40195327360314 (case), 10195327360313 (unit), Lot Numbers:  23EDA949, 23GDA203, 23HDB800, 23JDB140, 23KDA685, 23KDC088;   ee) REF DYNJ907158A, UDI/DI 40183489970402 (case), 10195327137038 (unit), Lot Numbers:  22EME052, 22FMG234, 22IMC193, 22IMH124, 22LME781, 23CMD417, 23CME132, 23CMF812, 23DMF106, 23GMB888, 23HMH494, 23IME266, 23JMA733, 23KMH135;   ff) REF CDS983991C, UDI/DI 40889942131410 (case), 10889942131419 (unit), Lot Numbers:  22FBB136, 22FBU282, 22GBN805, 22HBG300, 22HBS717, 22IBI043, 23CBT616, 23EBA215, 23EBU789, 23HBI490;   gg) REF DYNJ902367J, UDI/DI 40195327505838 (case), 10195327505837 (unit), Lot Numbers:  23JBG975, 23KBN775, 23KBP709;   hh) REF DYNJ905852C, UDI/DI 40195327214204 (case), 10195327214203 (unit), Lot Numbers:  22IBK464, 22IBM480, 23ABO113, 23ABO114, 23ABQ791, 23DBP733, 23EBR661, 23GBO389, 23HBX998, 23KBG164, 23LBF311;   ii) REF DYNJ905514D, UDI/DI 40193489968034 (case), 10193489968033 (unit), Lot Numbers:  22EMA529, 22EMH888, 22FMB880, 22GME946, 22GMH574, 22GMI092, 22HMH887, 22LMD324, 22LMI453, 23AMG866, 23IMG780. 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-2714-2024&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-2714-2024&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-2714-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-2714-2024 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-2714-2024&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-2714-2024&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-2714-2024/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."
    }
  ],
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            "Field": "Recall number",
            "Value": "Z-2714-2024",
            "Status": "recorded"
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          "item": {
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            "Field": "Status",
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            "Status": "recorded"
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          "item": {
            "Field": "Recalling firm",
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            "Status": "recorded"
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          "item": {
            "Field": "Reason",
            "Value": "A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.",
            "Status": "recorded"
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        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-03-22",
            "Status": "recorded"
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            "Field": "Distribution pattern",
            "Value": "Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.",
            "Status": "recorded"
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