{
  "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": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72035",
      "recalling_firm": "STERILMED, INC.",
      "address_1": "11400 73rd Ave N",
      "address_2": "N/A",
      "postal_code": "55369-5561",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of CA, KY, MI, OH, UT and  WI.",
      "recall_number": "Z-2819-2015",
      "product_description": "Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34\" Single Hose Single Bladder Brown (PLC), 34\",  Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed.    Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box. Each sales unit (casepack) contains 5 devices.",
      "product_quantity": "43",
      "reason_for_recall": "Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part #ZIM60-7075-106, lot number 1846885 due to mislabeling. The affected reprocessed product is labeled as single hose devices but the devices inside the packaging are dual hose devices.",
      "recall_initiation_date": "20150824",
      "center_classification_date": "20150928",
      "termination_date": "20160311",
      "report_date": "20151007",
      "code_info": "Lot 1846885"
    }
  ]
}