{
  "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": "86942",
      "recalling_firm": "Steris Corporation",
      "address_1": "5960 Heisley Rd",
      "address_2": "",
      "postal_code": "44060-1834",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:",
      "recall_number": "Z-0789-2021",
      "product_description": "Vis-U-All High Temperature Tubing 9\"x100'. One roll per box; 10 boxes per case 6 rolls/cs\t\t  Model Number: 881091",
      "product_quantity": "197 cases",
      "reason_for_recall": "Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch",
      "recall_initiation_date": "20201202",
      "center_classification_date": "20210107",
      "termination_date": "20220621",
      "report_date": "20210113",
      "code_info": "Lot Number: 200408A",
      "more_code_info": ""
    }
  ]
}