{
  "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,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88964",
      "recalling_firm": "Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "address_2": "",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Puerto Rico",
      "recall_number": "Z-0314-2022",
      "product_description": "28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122",
      "product_quantity": "",
      "reason_for_recall": "There is a potential for the outer white Tyvek lid to debond from the sealed package.",
      "recall_initiation_date": "20211015",
      "center_classification_date": "20211130",
      "report_date": "20211208",
      "code_info": "UDI number - (01) 07613327013016(17)261013(10);  lot numbers - 86604305, 86604306",
      "more_code_info": ""
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}