{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92460",
      "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": "There was no U.S. distribution, including government and military.    Foreign distribution was made to Australia, Belgium, Canada, Chile, China, Colombia, France, Germany, Italy, Mexico, Netherlands, Spain, Sweden, Switzerland, Taiwan, and the United Kingdom.",
      "recall_number": "Z-2105-2023",
      "product_description": "Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile.",
      "product_quantity": "106 devices",
      "reason_for_recall": "The devices were manufactured with the pin sleeve holes too narrow, which does not allow  the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.",
      "recall_initiation_date": "20230613",
      "center_classification_date": "20230706",
      "report_date": "20230712",
      "code_info": "Lot numbers 2656815 and 2762126, UDI-DI 00889797003926."
    }
  ]
}