{
  "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": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92138",
      "recalling_firm": "Stryker Sustainability Solutions",
      "address_1": "1810 W Drake Dr",
      "address_2": "N/A",
      "postal_code": "85283-4327",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US: WA OUS: None",
      "recall_number": "Z-1612-2023",
      "product_description": "REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12\", Rx Only Non-Sterile",
      "product_quantity": "50 units",
      "reason_for_recall": "Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be  mislabeled and/or mispackaged.",
      "recall_initiation_date": "20230414",
      "center_classification_date": "20230519",
      "report_date": "20230524",
      "code_info": "Lot # 0000157564, UDI-DI: 00885825013585"
    }
  ]
}