{
  "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": "89592",
      "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 Nationwide distribution in the states of AZ, CA, CO, FL, GA,  MD, MN, NC, NJ, NY, OH, OR, PA, TN, TX and the countries of Canada, China, Japan, Spain, UK, Netherlands, Germany & Belgium.   ***Updated 3/17/22: U.S., Canada, China, Japan, UK, and Netherlands.",
      "recall_number": "Z-0843-2022",
      "product_description": "Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm\t Catalog Number: 6570-0-232",
      "product_quantity": "39 units Updated: 40 units",
      "reason_for_recall": "Potential product mix where the size and/or offset of the Biolox delta Ceramic V40 Femoral Head inside the package does not match the package labeling",
      "recall_initiation_date": "20220114",
      "center_classification_date": "20220331",
      "report_date": "20220406",
      "code_info": "Lot Number: 89546202   GTIN: (01)04546540608536(17)261020(10)89546202"
    }
  ]
}