{
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    "supported": "au:supported",
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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1805-2024.jsonld",
  "@type": "schema:Dataset",
  "name": "Medtronic Venous Cannulae:    a)\tDLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,   b)\tDLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,   c)\tDLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128,   d)\tDLP¿ 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130,   e)\tDLP¿ 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134,   f)\tDLP¿ 12 Fr. Single Stage Venous Cannula, Model Number 67312,   g)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67316,   h)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67516,   i)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 66118,   j)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 67318,   k)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67320,   l)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 69320,   m)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67520,   n)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 66122,   o)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 67522,   p)\tDLP¿ 24 Fr. Single Stage Venous Cannula, Model Number 67524,   q)\tDLP¿ 26 Fr. Single Stage Venous Cannula, Model Number 67526,   r)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 66128,   s)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 39628,   t)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 67528,   u)\tDLP¿ 30 Fr. Single Stage Venous Cannula, Model Number 66130,   v)\tDLP¿ 31 Fr. Single Stage Venous Cannula, Model Number 69331,   w)\tDLP¿ 32 Fr. Single Stage Venous Cannula, Model Number 66132,   x)\tDLP¿ 34 Fr. Single Stage Venous Cannula, Model Number 67534,   y)\tDLP¿ 36 Fr. Single Stage Venous Cannula, Model Number 66236,   z)\tMC2¿ 28/36 Fr. Two Stage Venous Cannula, Model Number 91228,   aa)\tMC2¿ 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C,   bb) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263,   cc)\tMC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C,   dd) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C,   ee)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246,   ff)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C,   gg)\tMC2¿ 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C,   hh) MC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251,   ii)\tMC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C,   jj)\tVC2\" 34/38 Fr. Venous Cannula, Model Number 93438,   kk)\tVC2\" 34/48 Fr. Venous Cannula, Model Number 93448C",
  "description": "FDA recall Z-1805-2024 — Medtronic Perfusion Systems is recalling Medtronic Venous Cannulae:    a)\tDLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,   b)\tDLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,   c)\tDLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128,   d)\tDLP¿ 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130,   e)\tDLP¿ 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134,   f)\tDLP¿ 12 Fr. Single Stage Venous Cannula, Model Number 67312,   g)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67316,   h)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67516,   i)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 66118,   j)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 67318,   k)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67320,   l)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 69320,   m)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67520,   n)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 66122,   o)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 67522,   p)\tDLP¿ 24 Fr. Single Stage Venous Cannula, Model Number 67524,   q)\tDLP¿ 26 Fr. Single Stage Venous Cannula, Model Number 67526,   r)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 66128,   s)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 39628,   t)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 67528,   u)\tDLP¿ 30 Fr. Single Stage Venous Cannula, Model Number 66130,   v)\tDLP¿ 31 Fr. Single Stage Venous Cannula, Model Number 69331,   w)\tDLP¿ 32 Fr. Single Stage Venous Cannula, Model Number 66132,   x)\tDLP¿ 34 Fr. Single Stage Venous Cannula, Model Number 67534,   y)\tDLP¿ 36 Fr. Single Stage Venous Cannula, Model Number 66236,   z)\tMC2¿ 28/36 Fr. Two Stage Venous Cannula, Model Number 91228,   aa)\tMC2¿ 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C,   bb) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263,   cc)\tMC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C,   dd) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C,   ee)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246,   ff)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C,   gg)\tMC2¿ 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C,   hh) MC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251,   ii)\tMC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C,   jj)\tVC2\" 34/38 Fr. Venous Cannula, Model Number 93438,   kk)\tVC2\" 34/48 Fr. Venous Cannula, Model Number 93448C (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.",
  "license": "https://creativecommons.org/publicdomain/zero/1.0/",
  "isAccessibleForFree": true,
  "isPartOf": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
  "rdfs:isDefinedBy": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
  "isBasedOn": {
    "@type": "schema:Dataset",
    "name": "openFDA drug & device enforcement (recall) reports",
    "url": "https://open.fda.gov/apis/drug/enforcement/",
    "creator": {
      "@type": "schema:GovernmentOrganization",
      "name": "U.S. Food & Drug Administration"
    }
  },
  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1805-2024&lang=eng",
  "about": {
    "@type": "schema:MedicalDevice",
    "name": "Medtronic Venous Cannulae:    a)\tDLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,   b)\tDLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,   c)\tDLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128,   d)\tDLP¿ 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130,   e)\tDLP¿ 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134,   f)\tDLP¿ 12 Fr. Single Stage Venous Cannula, Model Number 67312,   g)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67316,   h)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67516,   i)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 66118,   j)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 67318,   k)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67320,   l)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 69320,   m)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67520,   n)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 66122,   o)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 67522,   p)\tDLP¿ 24 Fr. Single Stage Venous Cannula, Model Number 67524,   q)\tDLP¿ 26 Fr. Single Stage Venous Cannula, Model Number 67526,   r)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 66128,   s)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 39628,   t)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 67528,   u)\tDLP¿ 30 Fr. Single Stage Venous Cannula, Model Number 66130,   v)\tDLP¿ 31 Fr. Single Stage Venous Cannula, Model Number 69331,   w)\tDLP¿ 32 Fr. Single Stage Venous Cannula, Model Number 66132,   x)\tDLP¿ 34 Fr. Single Stage Venous Cannula, Model Number 67534,   y)\tDLP¿ 36 Fr. Single Stage Venous Cannula, Model Number 66236,   z)\tMC2¿ 28/36 Fr. Two Stage Venous Cannula, Model Number 91228,   aa)\tMC2¿ 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C,   bb) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263,   cc)\tMC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C,   dd) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C,   ee)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246,   ff)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C,   gg)\tMC2¿ 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C,   hh) MC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251,   ii)\tMC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C,   jj)\tVC2\" 34/38 Fr. Venous Cannula, Model Number 93438,   kk)\tVC2\" 34/48 Fr. Venous Cannula, Model Number 93448C",
    "manufacturer": {
      "@type": "schema:Organization",
      "name": "Medtronic Perfusion Systems"
    }
  },
  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1805-2024/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-1805-2024: Medtronic Perfusion Systems is recalling Medtronic Venous Cannulae:    a)\tDLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,   b)\tDLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,   c)\tDLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128,   d)\tDLP¿ 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130,   e)\tDLP¿ 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134,   f)\tDLP¿ 12 Fr. Single Stage Venous Cannula, Model Number 67312,   g)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67316,   h)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67516,   i)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 66118,   j)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 67318,   k)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67320,   l)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 69320,   m)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67520,   n)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 66122,   o)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 67522,   p)\tDLP¿ 24 Fr. Single Stage Venous Cannula, Model Number 67524,   q)\tDLP¿ 26 Fr. Single Stage Venous Cannula, Model Number 67526,   r)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 66128,   s)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 39628,   t)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 67528,   u)\tDLP¿ 30 Fr. Single Stage Venous Cannula, Model Number 66130,   v)\tDLP¿ 31 Fr. Single Stage Venous Cannula, Model Number 69331,   w)\tDLP¿ 32 Fr. Single Stage Venous Cannula, Model Number 66132,   x)\tDLP¿ 34 Fr. Single Stage Venous Cannula, Model Number 67534,   y)\tDLP¿ 36 Fr. Single Stage Venous Cannula, Model Number 66236,   z)\tMC2¿ 28/36 Fr. Two Stage Venous Cannula, Model Number 91228,   aa)\tMC2¿ 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C,   bb) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263,   cc)\tMC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C,   dd) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C,   ee)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246,   ff)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C,   gg)\tMC2¿ 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C,   hh) MC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251,   ii)\tMC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C,   jj)\tVC2\" 34/38 Fr. Venous Cannula, Model Number 93438,   kk)\tVC2\" 34/48 Fr. Venous Cannula, Model Number 93448C",
      "text": "The FDA logged enforcement record Z-1805-2024: Medtronic Perfusion Systems is voluntarily recalling Medtronic Venous Cannulae:    a)\tDLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120,   b)\tDLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124,   c)\tDLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128,   d)\tDLP¿ 30 Fr. Malleable Single Stage Venous Cannula, Model Number 68130,   e)\tDLP¿ 34 Fr. Malleable Single Stage Venous Cannula, Model Number 68134,   f)\tDLP¿ 12 Fr. Single Stage Venous Cannula, Model Number 67312,   g)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67316,   h)\tDLP¿ 16 Fr. Single Stage Venous Cannula, Model Number 67516,   i)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 66118,   j)\tDLP¿ 18 Fr. Single Stage Venous Cannula, Model Number 67318,   k)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67320,   l)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 69320,   m)\tDLP¿ 20 Fr. Single Stage Venous Cannula, Model Number 67520,   n)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 66122,   o)\tDLP¿ 22 Fr. Single Stage Venous Cannula, Model Number 67522,   p)\tDLP¿ 24 Fr. Single Stage Venous Cannula, Model Number 67524,   q)\tDLP¿ 26 Fr. Single Stage Venous Cannula, Model Number 67526,   r)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 66128,   s)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 39628,   t)\tDLP¿ 28 Fr. Single Stage Venous Cannula, Model Number 67528,   u)\tDLP¿ 30 Fr. Single Stage Venous Cannula, Model Number 66130,   v)\tDLP¿ 31 Fr. Single Stage Venous Cannula, Model Number 69331,   w)\tDLP¿ 32 Fr. Single Stage Venous Cannula, Model Number 66132,   x)\tDLP¿ 34 Fr. Single Stage Venous Cannula, Model Number 67534,   y)\tDLP¿ 36 Fr. Single Stage Venous Cannula, Model Number 66236,   z)\tMC2¿ 28/36 Fr. Two Stage Venous Cannula, Model Number 91228,   aa)\tMC2¿ 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C,   bb) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263,   cc)\tMC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C,   dd) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C,   ee)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246,   ff)\tMC2¿ 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C,   gg)\tMC2¿ 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C,   hh) MC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251,   ii)\tMC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C,   jj)\tVC2\" 34/38 Fr. Venous Cannula, Model Number 93438,   kk)\tVC2\" 34/48 Fr. Venous Cannula, Model Number 93448C — reason: Potential for unsealed sterile packing.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-03-19. Affected lots/codes: a) Model Number 68120, GTIN 20613994879435, Lot Numbers:  2023041436;    b) Model Number 68124, GTIN 00613994879417, Lot Numbers:  2023041441, 2023041448;  b) Model Number 68124, GTIN 00681490466349, Lot Numbers:  2023041441, 2023041448;  b) Model Number 68124, GTIN 20613994879411, Lot Numbers:  2023041441, 2023041448, 202306C008;  c) Model Number 68128, GTIN 00613994879394, Lot Numbers:  2023041040;  c) Model Number 68128, GTIN 00681490466363, Lot Numbers:  2023041388;  c) Model Number 68128, GTIN 20613994879398, Lot Numbers:  2023041040, 2023041388, 202306C010, 202306C011;  d) Model Number 68130, GTIN  20613994879381, Lot Numbers:  2023041390, 202308C131;  e) Model Number 68134, GTIN 20613994879367, Lot Numbers:  2023041431;  f) Model Number 67312, GTIN 00613994879325, Lot Numbers:  2023041423;  f) Model Number 67312, GTIN 00673978184180, Lot Numbers:  2023040074;  f) Model Number 67312, GTIN 20613994879329, Lot Numbers:  2023040073, 2023040074, 2023041423;  g) Model Number 67316, GTIN 00613994879301, Lot Numbers:  2023040076, 2023041416;  g) Model Number 67316, GTIN 20613994879305, Lot Numbers:  2023040076, 2023041416, 202305C264;  h) Model Number 67516, GTIN 00613994879301, Lot Numbers:  2023040076, 2023041416;  h) Model Number 67516, GTIN 20613994879305, Lot Numbers:  2023040076, 2023041416, 202305C264;  i) Model Number 66118, GTIN 00613994878526, Lot Numbers:  2023041014;  i) Model Number 66118, GTIN 20613994878520, Lot Numbers:  2023041014, 2023041015;  j) Model Number 67318, GTIN 00613994879295, Lot Numbers:  2023040077;  j) Model Number 67318, GTIN 00673978184241, Lot Numbers:  2023040077, 2023041391;  j) Model Number 67318, GTIN 20613994879299, Lot Numbers:  2023040077, 2023041391, 202305C256;  k) Model Number 67320, GTIN 00613994879288, Lot Numbers:  2023031377;  k) Model Number 67320, GTIN 00673978184258, Lot Numbers:  2023031377;  k) Model Number 67320, GTIN 20613994879282, Lot Numbers:  2023031377, 202307C051;  l) Model Number 69320, GTIN 00613994879233, Lot Numbers:  2023041422;  l) Model Number 69320, GTIN 00673978184609, Lot Numbers:  2023041422;  l) Model Number 69320, GTIN 20613994879237, Lots Numbers:  2023041422, 2023041438, 202306C014, 202306C015;  m) Model Number 67520, GTIN 00613994878359, Lot Numbers:  2023040082;  m) Model Number 67520, GTIN 20613994878353, Lot Numbers:  2023040082;  n) Model Number 66122, GTIN 20613994878544, Lot Numbers:  2023041016;  o) Model Number 67522, GTIN 00613994878366, Lot Numbers:  2023040083, 2023040565;  o) Model Number 67522, GTIN 00673978184326, Lot Numbers:  2023040083, 2023040565;  o) Model Number 67522, GTIN 20613994878360, Lot Numbers:  2023040083, 2023040565, 202307C050;  p) Model Number 67524, GTIN 00673978184333, Lot Numbers:  2023040084;  p) Model Number 67524, GTIN 20613994878377, Lot Numbers:  2023040084, 2023040566, 202305C257;  q) Model Number 67526, GTIN 00673978165585, Lot Numbers:  2023040569;  q) Model Number 67526, GTIN 20613994878384, Lot Numbers:  2023040569, 202308C082;  r) Model Number 66128, GTIN 00613994878571, Lot Numbers:  2023041020;  r) Model Number 66128, GTIN 20613994878575, Lot Numbers:  2023041020, 202305C177;  s) Model Number 39628, GTIN  t) Model Number 67528, GTIN 20613994878391, Lot Numbers:  2023041036;  u) Model Number 66130, GTIN 00613994878588, Lot Numbers:  2023040555, 202305C217;  u) Model Number 66130, GTIN 20613994878582, Lot Numbers:  2023040555, 2023041414, 202305C217, 202305C218;  v) Model Number 69331, GTIN 20613994879183, Lot Numbers:  2023041444, 202307C012;  w) Model Number 66132, GTIN 00613994878601, Lot Numbers:  2023041428;  w) Model Number 66132, GTIN 20613994878605, Lot Numbers:  2023041412, 2023041428, 202305C227;  x) Model Number 67534, GTIN 20613994878421, Lot Numbers:  2023031249, 202308C079;  y) Model Number 66236, GTIN 20613994878643, Lot Numbers:  2023041398, 202305C222;  z) Model Number 91228, GTIN 20643169463015, Lot Numbers:  2023041070;  aa) Model Number 91229C, GTIN 20643169463060, Lot Numbers:  2023041071;  bb) Model Number 91263, GTIN 00673978187761, Lot Numbers:  2023041095;  bb) Model Number 91263, GTIN 20613994887454, Lot Numbers:  2023041095, 202306C105;  cc) Model Number 91240C, GTIN 00613994887306, Lot Numbers:  2023041082, 2023041083, 2023041084;  cc) Model Number 91240C, GTIN 20613994887300, Lot Numbers:  2023041079, 2023041081, 2023041082, 2023041083, 2023041084, 2023041087, 2023041088, 202306C074, 202306C075, 202306C076, 202306C077;  dd) Model Number 91263C, GTIN 20613994887447, Lot Numbers:  2023040116, 2023041097, 202306C103;  ee) Model Number 91246, GTIN 00613994887535, Lot Numbers:    2023041089;  ee) Model Number 91246, GTIN 20613994887539, Lot Numbers:  2023041089, 202306C101;  ff) Model Number 91246C, GTIN 00613994887528, Lot Numbers:  2023041090;  ff) Model Number 91246C, GTIN 20613994887522, Lot Numbers:  2023041090, 202306C123;  gg) Model Number 91236C, GTIN 00613994887344, Lot Numbers:  2023041072;  gg) Model Number 91236C, GTIN 20613994887348, Lot Numbers:  2023041072, 202306C065;  hh) Model Number 91251, GTIN 00613994887498, Lot Numbers:  2023041092, 2023041094;  hh) Model Number 91251, GTIN 20613994887492, Lot Numbers:  2023041092, 2023041094;  ii) Model Number 91251C, GTIN 00613994887481, Lot Numbers:  2023040618, 202306C102;  ii) Model Number 91251C, GTIN 20613994887485, Lot Numbers:  2023040617, 2023040618, 202306C102;  jj) Model Number 93438, GTIN 00673978188201, Lot Numbers:  2023040626;  jj) Model Number 93438, GTIN 20613994887034, Lot Numbers:  2023040626;  kk) Model Number 93448C, GTIN  20613994887256, Lot Numbers:  2023040627. 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-1805-2024&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-1805-2024&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-1805-2024/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1805-2024 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-1805-2024&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-1805-2024&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-1805-2024/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": {
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        "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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          "item": {
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            "Status": "recorded"
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          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Potential for unsealed sterile packing.",
            "Status": "recorded"
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          "position": 7,
          "item": {
            "Field": "Initiated",
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