{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68418",
      "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 Nationwide Distribution in the state of California",
      "recall_number": "Z-1925-2014",
      "product_description": "DISCOVERY ELBOW prosthesis, 4 MM X 100 MM RIGHT HUMERAL FLANGED I BOND COAT Tl 6AL 4V ALLOY.                      Elbow joint replacement prostheses are intended for primary and revision joint arthroplasty for use in cemented applications.",
      "product_quantity": "1",
      "reason_for_recall": "Surface finish is different than specified.  The implant has 30 grit blast on the exterior of the flange when the print calls for the glass bead blast.  The patient may experience pain requiring surgical intervention.",
      "recall_initiation_date": "20140515",
      "center_classification_date": "20140626",
      "termination_date": "20150316",
      "report_date": "20140702",
      "code_info": "Catalog/REF #: 114905, Lot #: M846640"
    }
  ]
}