{
  "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": "2026-04-01",
    "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": "87230",
      "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": "Domestic: AL, AK, AR, AZ, CA, CO, CT, DC, FL, GA, ID, IL IN, IW, KS, KY, LA, ME, MD, MI, MN, MO, NE, NV, NJ, NY, NC, ND, OH, OK, OR, PA, PR, SC, TX, UT, VT, VA, WA, WV, WI. Foreign: Canada, South Korea, Panama, Qatar, Thailand.",
      "recall_number": "Z-1149-2021",
      "product_description": "OT1000 Series Orthopedic Surgical Tables",
      "product_quantity": "272 tables total (Domestic: 227 tables, Foreign 45 tables)",
      "reason_for_recall": "On January 7, 2021, STERIS identified that the glued bond between the beam and the leg spar assembly may begin to separate over time.  This could result in unexpected movement of the affected leg spar if the separation occurred during a patient procedure.",
      "recall_initiation_date": "20210121",
      "center_classification_date": "20210224",
      "termination_date": "20211110",
      "report_date": "20210303",
      "code_info": "Model No.: OT1000, OT1100, OT1200"
    }
  ]
}