{
  "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": "66792",
      "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": "Worldwide Distribution: USA (nationwide) and Internationally to Japan.",
      "recall_number": "Z-0381-2014",
      "product_description": "REF 200068 Security (TM) Enclosed Carpal Tunnel System  Blade ( Single) ABS /Stainless Steel  Sterile Device,  Single Use Only.     Designed to release the transverse carpal ligament.",
      "product_quantity": "1130",
      "reason_for_recall": "Security Blades were manufactured oversized and potentially won't advance or may be difficult to advance through the mating Security Clip.",
      "recall_initiation_date": "20131025",
      "center_classification_date": "20131122",
      "termination_date": "20150506",
      "report_date": "20131204",
      "code_info": "Catalog Number: 200068  Medical Device Listing Number: B008657  Lot Number Identification: 088610, 090600, 143810, 257060, 289900, 365910, 460490, 558300, 626660,  697320,767260,795090,857730,864640,979680"
    }
  ]
}