{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91716",
      "recalling_firm": "Stryker Medical Division of Stryker Corporation",
      "address_1": "3800 E Centre Ave",
      "address_2": "N/A",
      "postal_code": "49002-5826",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of NY, VA.",
      "recall_number": "Z-1256-2023",
      "product_description": "Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location.  Model: 650705550001",
      "product_quantity": "4 units",
      "reason_for_recall": "Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.",
      "recall_initiation_date": "20230201",
      "center_classification_date": "20230315",
      "report_date": "20230322",
      "code_info": "GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664"
    }
  ]
}