{
  "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": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89456",
      "recalling_firm": "Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Puerto Rico and the countries of Canada, and Malaysia.",
      "recall_number": "Z-0644-2022",
      "product_description": "32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032",
      "product_quantity": "8 units",
      "reason_for_recall": "There is a potential for the outer Tyvek lid to de-bond from the sealed package.",
      "recall_initiation_date": "20211221",
      "center_classification_date": "20220216",
      "report_date": "20220223",
      "code_info": "UDI: 07613327012842;  Lot Number: 87327407"
    }
  ]
}