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  "name": "Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemostat, REF G21049, 3.7 mm, Sterile. The device is used for hemostasis of nonvariceal gastrointestinal bleeding.",
  "description": "FDA recall Z-0036-2025 — Wilson-Cook Medical Inc. is recalling Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemostat, REF G21049, 3.7 mm, Sterile. The device is used for hemostasis of nonvariceal gastrointestinal bleeding. (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/",
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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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    "name": "openFDA drug & device enforcement (recall) reports",
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0036-2025&lang=eng",
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    "@type": "schema:MedicalDevice",
    "name": "Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemostat, REF G21049, 3.7 mm, Sterile. The device is used for hemostasis of nonvariceal gastrointestinal bleeding.",
    "manufacturer": {
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      "name": "Wilson-Cook Medical Inc."
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  "claims": [
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0036-2025/enforcement-record",
      "@type": "schema:Claim",
      "name": "FDA recall Z-0036-2025: Wilson-Cook Medical Inc. is recalling Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemostat, REF G21049, 3.7 mm, Sterile. The device is used for hemostasis of nonvariceal gastrointestinal bleeding.",
      "text": "The FDA logged enforcement record Z-0036-2025: Wilson-Cook Medical Inc. is voluntarily recalling Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemostat, REF G21049, 3.7 mm, Sterile. The device is used for hemostasis of nonvariceal gastrointestinal bleeding. — reason: Specific lots of product have been manufactured with nonconforming raw materials.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-08-29. Affected lots/codes: HEMO-7, REF G56572 - UDI-DI 00827002565722; Lot numbers: W4849600, exp. 6/27/2027; W4849968, exp. 6/28/2027; W4849969, exp. 6/28/2027; W4849970, exp. 6/28/2027; W4849971, exp. 6/28/2027; W4849972, exp. 6/28/2027; W4850219, exp. 7/1/2027; W4850220, exp. 7/1/2027;  W4850221, exp. 7/1/2027; W4850659, exp. 7/2/2027; W4850660, exp. 7/2/2027; W4850662, exp. 7/2/2027; W4851084, exp. 7/3/2027; W4851085, exp. 7/3/2027; W4851086, 7/3/2027; W4852285, exp. 7/10/2027; and W4852286, exp. 7/10/2027; and  HEMO-10, REF G21049 - UDI-DI 00827002210493; Lot numbers: W4849973, exp. 6/28/2027; and W4850217, exp. 7/1/2027.  UPDATED 11/4/2024 FOR EXPANSION OF LOT NUMBERS:  HEMO-7, REF G56572:  Lot numbers: W4843115, W4843116, W4843117, W4843118, W4843119, W4849594, W4849595, W4849596, W4849597, W4849599, W4851251, W4851252, W4851253, W4851254, W4851255, W4851256, W4851257, W4851590, W4851591, W4851592, W4851596, W4851660, W4851871, W4851872, W4851874, W4851876, W4851877, W4851878, W4851879, W4851880, W4852627, W4852628, W4853096, W4853097, W4853098, W4853099, W4853100, W4853101, W4853102, W4853104, W4853105, W4853462, W4853463, W4853464, W4853465, W4853468, W4853469, W4859532, W4859533, W4859891, W4859892, W4859894, W4859895, W4859896, W4859897, W4859898, W4859899, W4860112, W4853470, W4853471, W4853948, W4853949, W4853950, W4853952, W4853954, W4854699, W4854700, W4854702, W4854703, W4854704, W4854705, W4854706, W4855265, W4855266, W4855267, W4855269, W4855270, W4855271, W4855272, W4855696, W4855697, W4855701, W4856471, W4856889, W4856892, W4856893, W4856894, W4856895, W4857327, W4857719, W4858445, W4858449, W4858450, W4858452, W4858454, W4858869, W4859152, W4859529, W4859530, W4859531, W4845546, W4845880, W4845881, W4845882, W4845883, W4845884, W4845886, W4845889, W4846299, W4846301, W4846303, W4847081, W4847085, W4847495, W4847496, W4847497, W4847498, W4847499, W4847500, W4847504, W4847892, W4847893, W4847894, W4847896, W4848132, W4848709, W4848710, W4848711, W4848712, W4848713, W4848714, W4848715, W4848716, W4848717, W4849067, W4849068, W4849070, W4849071, W4849072, W4849074, W4849075, W4849593, W4843512, W4843513, W4843514, W4843515, W4843516, W4843517, W4843518, W4843520, W4843860, W4843861, W4843862, W4843863, W4843865, W4843867, W4843868, W4843869, W4844246, W4844247, W4844248, W4844249, W4844251, W4844252, W4844253, W4844254, W4844643, W4844644, W4844646, W4844647, W4844649, W4844651, W4845120, W4845121, W4845122, W4845124, W4845125, W4845538, W4845539, W4845540, W4845541, W4845542, W4845543, and W4845545.  HEMO-10, REF G21049, Lot numbers:  W4843112, W4843113, W4843519, W4843864, W4843866, W4844250, W4844645, W4845117, W4845537, W4845544, W4845885, W4845888, W4847502, W4847503, W4848136, W4848708, W4849066, W4849069, W4849592, W4849598, W4851258, W4851593, W4851873, W4852282, W4853103, W4853467, W4853945, W4854701, W4855273, W4855699, W4858447, W4858868, W4859528, W4859890, W4859893, W4860295, and W4860304.  UPDATE FROM 1/20/2025 EXPANSION:  HEMO-7, REF G56572 - Lot numbers W4845123, W4843511, and W4845887.. A RECORDED FDA enforcement action (occurred=true).",
      "claimType": "official_fact",
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        "adjudged": true,
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        "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-0036-2025&lang=eng",
        "value": "Devices recall, status Ongoing",
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          "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-0036-2025&lang=eng"
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      "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-0036-2025/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-0036-2025 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
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      "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-0036-2025&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-0036-2025&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-0036-2025/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
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      "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-0036-2025",
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          "position": 1,
          "item": {
            "Field": "Recall number",
            "Value": "Z-0036-2025",
            "Status": "recorded"
          }
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          "position": 2,
          "item": {
            "Field": "Product type",
            "Value": "Devices",
            "Status": "recorded"
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          "position": 3,
          "item": {
            "Field": "Classification",
            "Value": "Class II",
            "Status": "determination"
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          "position": 4,
          "item": {
            "Field": "Status",
            "Value": "Ongoing — the recall is still being carried out.",
            "Status": "recorded"
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        {
          "@type": "schema:ListItem",
          "position": 5,
          "item": {
            "Field": "Recalling firm",
            "Value": "Wilson-Cook Medical Inc.",
            "Status": "recorded"
          }
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        {
          "@type": "schema:ListItem",
          "position": 6,
          "item": {
            "Field": "Reason",
            "Value": "Specific lots of product have been manufactured with nonconforming raw materials.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 7,
          "item": {
            "Field": "Initiated",
            "Value": "2024-08-29",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 8,
          "item": {
            "Field": "Lot/code info",
            "Value": "HEMO-7, REF G56572 - UDI-DI 00827002565722; Lot numbers: W4849600, exp. 6/27/2027; W4849968, exp. 6/28/2027; W4849969, exp. 6/28/2027; W4849970, exp. 6/28/2027; W4849971, exp. 6/28/2027; W4849972, exp. 6/28/2027; W4850219, exp. 7/1/2027; W4850220, exp. 7/1/2027;  W4850221, exp. 7/1/2027; W4850659, exp. 7/2/2027; W4850660, exp. 7/2/2027; W4850662, exp. 7/2/2027; W4851084, exp. 7/3/2027; W4851085, exp. 7/3/2027; W4851086, 7/3/2027; W4852285, exp. 7/10/2027; and W4852286, exp. 7/10/2027; and  HEMO-10, REF G21049 - UDI-DI 00827002210493; Lot numbers: W4849973, exp. 6/28/2027; and W4850217, exp. 7/1/2027.  UPDATED 11/4/2024 FOR EXPANSION OF LOT NUMBERS:  HEMO-7, REF G56572:  Lot numbers: W4843115, W4843116, W4843117, W4843118, W4843119, W4849594, W4849595, W4849596, W4849597, W4849599, W4851251, W4851252, W4851253, W4851254, W4851255, W4851256, W4851257, W4851590, W4851591, W4851592, W4851596, W4851660, W4851871, W4851872, W4851874, W4851876, W4851877, W4851878, W4851879, W4851880, W4852627, W4852628, W4853096, W4853097, W4853098, W4853099, W4853100, W4853101, W4853102, W4853104, W4853105, W4853462, W4853463, W4853464, W4853465, W4853468, W4853469, W4859532, W4859533, W4859891, W4859892, W4859894, W4859895, W4859896, W4859897, W4859898, W4859899, W4860112, W4853470, W4853471, W4853948, W4853949, W4853950, W4853952, W4853954, W4854699, W4854700, W4854702, W4854703, W4854704, W4854705, W4854706, W4855265, W4855266, W4855267, W4855269, W4855270, W4855271, W4855272, W4855696, W4855697, W4855701, W4856471, W4856889, W4856892, W4856893, W4856894, W4856895, W4857327, W4857719, W4858445, W4858449, W4858450, W4858452, W4858454, W4858869, W4859152, W4859529, W4859530, W4859531, W4845546, W4845880, W4845881, W4845882, W4845883, W4845884, W4845886, W4845889, W4846299, W4846301, W4846303, W4847081, W4847085, W4847495, W4847496, W4847497, W4847498, W4847499, W4847500, W4847504, W4847892, W4847893, W4847894, W4847896, W4848132, W4848709, W4848710, W4848711, W4848712, W4848713, W4848714, W4848715, W4848716, W4848717, W4849067, W4849068, W4849070, W4849071, W4849072, W4849074, W4849075, W4849593, W4843512, W4843513, W4843514, W4843515, W4843516, W4843517, W4843518, W4843520, W4843860, W4843861, W4843862, W4843863, W4843865, W4843867, W4843868, W4843869, W4844246, W4844247, W4844248, W4844249, W4844251, W4844252, W4844253, W4844254, W4844643, W4844644, W4844646, W4844647, W4844649, W4844651, W4845120, W4845121, W4845122, W4845124, W4845125, W4845538, W4845539, W4845540, W4845541, W4845542, W4845543, and W4845545.  HEMO-10, REF G21049, Lot numbers:  W4843112, W4843113, W4843519, W4843864, W4843866, W4844250, W4844645, W4845117, W4845537, W4845544, W4845885, W4845888, W4847502, W4847503, W4848136, W4848708, W4849066, W4849069, W4849592, W4849598, W4851258, W4851593, W4851873, W4852282, W4853103, W4853467, W4853945, W4854701, W4855273, W4855699, W4858447, W4858868, W4859528, W4859890, W4859893, W4860295, and W4860304.  UPDATE FROM 1/20/2025 EXPANSION:  HEMO-7, REF G56572 - Lot numbers W4845123, W4843511, and W4845887.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "Distribution was nationwide.  There was government and military distribution.  Foreign distribution was made to Canada, Costa Rica, and Guatemala.  UPDATE 1/30/2025:  Foreign distribution was made to:  Australia, Austria, Belgium, Canada, Chile, Costa Rica, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Guatemala, Hong Kong, Ireland, Italy, Latvia, Luxembourg, Mexico, Myanmar, Netherlands, Norway, New Zealand, Poland, Portugal, Romania, Singapore, Spain, Sweden, Switzerland, Thailand, and United Kingdom.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}