{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93486",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US States: AL, CA, MD, MI, NC, OH, OK, TN, TX. Netherlands.",
      "recall_number": "Z-0570-2024",
      "product_description": "Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02",
      "product_quantity": "10 units",
      "reason_for_recall": "One product complaint was received reporting that there was an incorrect adapter in the packaging. An adapter with neck length M/+0 was inside the product packaging, which should have contained an adapter with neck length S/-3.0. The difference in neck length may be recognized by the size (S or M) indicator on the device.",
      "recall_initiation_date": "20231102",
      "center_classification_date": "20231218",
      "report_date": "20231227",
      "code_info": "UDI-DI: 00889024430563; Lot Number: 3145300"
    }
  ]
}