{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91673",
      "recalling_firm": "Wright Medical Technology, Inc.",
      "address_1": "1023 Cherry Rd",
      "address_2": "N/A",
      "postal_code": "38117-5423",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of NY.",
      "recall_number": "Z-1169-2023",
      "product_description": "ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device",
      "product_quantity": "10 units",
      "reason_for_recall": "Stryker has identified an issue that impacts two specific lots of CLAW\" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa.",
      "recall_initiation_date": "20230202",
      "center_classification_date": "20230224",
      "report_date": "20230308",
      "code_info": "GTIN 00840420152985, Lot Number 1636048",
      "more_code_info": ""
    }
  ]
}