{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "3.5mmx38mm Locking Cortical Screw, implants are being recalled since an investigation identified  that a 3.5mmx28mm Cortical Locking Screw is labeled as a 3.5mmx38mm Cortical Locking Screw.",
      "address_2": "",
      "product_quantity": "52",
      "code_info": "Catalog Number: 816135038 (8161-35-038)  Lot Number Identification: RM244D",
      "center_classification_date": "20140110",
      "distribution_pattern": "US Distribution including states of: AZ, CA, GA, IL, KY, MI, NC, NH, NY, OH, PA, SD, TX, UT, and VA.",
      "state": "IN",
      "product_description": "Locking Cortical Screw  3.5mmX38mm  REF 8161-35-038",
      "report_date": "20140122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet, Inc.",
      "recall_number": "Z-0716-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67142",
      "termination_date": "20150707",
      "more_code_info": "",
      "recall_initiation_date": "20131219",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}