{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mentor",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74264",
      "recalling_firm": "Steris Corporation",
      "address_1": "5960 Heisley Rd",
      "address_2": "N/A",
      "postal_code": "44060-1834",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL;AK, AZ; AR; CA; CO; CT; DC; FL; GA; IL; IN; IA; NY; NJ; NC; OH; OK; OR; PA; PR; SC; TX; UT and  VA.   Foreign accounts: Canada; France; Korea; Panama; Qatar and Thailand.",
      "recall_number": "Z-2248-2016",
      "product_description": "OT1000 Series Orthopedic Surgical Tables",
      "product_quantity": "148",
      "reason_for_recall": "STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly.",
      "recall_initiation_date": "20160523",
      "center_classification_date": "20160720",
      "termination_date": "20160822",
      "report_date": "20160727",
      "code_info": "OT1000, OT1100, and OT1200 Orthopedic Surgical Table",
      "more_code_info": ""
    }
  ]
}