{
  "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": "South Jordan",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86831",
      "recalling_firm": "Merit Medical Systems, Inc.",
      "address_1": "1600 W Merit Pkwy",
      "address_2": "N/A",
      "postal_code": "84095-2416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to: KY, RI, and MD",
      "recall_number": "Z-0749-2021",
      "product_description": "Product Code: K05T-02533, Custom Inflation Kit, Custom K05 Sterile EO, Rx Only, (01)00884450255803    For Angiography/angioplasty.    The contents of the kit include surgical drapes, towels, medicine cups, needles, various bowls, pen and label sets (PAL), scalpel, several syringes, table covers, stopcocks, inflation device, and gauze",
      "product_quantity": "90 kits",
      "reason_for_recall": "Angiography/Angioplasty custom kits contain header bags which may not be fully sealed, resulting in a  compromised sterile barrier.  This could result in exposure to non-sterile devices which may lead to an infection requiring medical treatment.",
      "recall_initiation_date": "20201110",
      "center_classification_date": "20201229",
      "termination_date": "20221005",
      "report_date": "20210106",
      "code_info": "(01)00884450255803     Lot # T1883210"
    }
  ]
}