{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91849",
      "recalling_firm": "Stryker Corporation",
      "address_1": "1941 Stryker Way",
      "address_2": "",
      "postal_code": "49002-9711",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1344-2023",
      "product_description": "Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4,1BLA,2PRT QUICK  Catalog number: 5921-218-235NS    Indicated for use in surgical procedures that require the temporary occlusion of blood flow in a patient s extremities",
      "product_quantity": "1707 units (packs of 10)",
      "reason_for_recall": "Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, may lead to operative site blood loss, hemorrhage or, in exceedingly rare situations, other major complications",
      "recall_initiation_date": "20230301",
      "center_classification_date": "20230404",
      "report_date": "20230412",
      "code_info": "GTIN: 07613327606164 Lot Numbers: 2022111802 2022112904 2022121301 2022121302 2022121905 2022121906 2022121907 2022121908",
      "more_code_info": ""
    }
  ]
}