{
  "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": "2026-04-29",
    "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": "64354",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - No USA distribution -Internationally to Canada, Japan, and Chile",
      "recall_number": "Z-0925-2013",
      "product_description": "REF S313152 Straight Acetabular Inserter Handle Ringloc  non-sterile    Orthopedic manual surgical instrument",
      "product_quantity": "58",
      "reason_for_recall": "The Straight Ringloc Button Latch Inserter Handle may have been manufactured at the higher end of the tolerance causing interference with the Ringloc cup. The inserter handle may lock onto the cup during impaction.  If alternative inserters are not available this could cause a surgical delay greater than 30 minutes.",
      "recall_initiation_date": "20130205",
      "center_classification_date": "20130308",
      "termination_date": "20130930",
      "report_date": "20130320",
      "code_info": "Catalog Number 5313152  Lot 153880,153930, 415500, 648010",
      "more_code_info": ""
    }
  ]
}