{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89535",
      "recalling_firm": "Stryker Sustainability Solutions",
      "address_1": "1810 W Drake Dr",
      "address_2": "",
      "postal_code": "85283-4327",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: KS OK TX  OUS: None",
      "recall_number": "Z-0664-2022",
      "product_description": "REF: 5921-018-135, Stryker Color Cuff, 18\" (Red), Quick Connect Single Port, Single Bladder",
      "product_quantity": "40 units",
      "reason_for_recall": "Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder inflatable cuffs.",
      "recall_initiation_date": "20220121",
      "center_classification_date": "20220222",
      "termination_date": "20250226",
      "report_date": "20220302",
      "code_info": "Lot # 12983349",
      "more_code_info": ""
    }
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}