{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91350",
      "recalling_firm": "Stradis Healthcare",
      "address_1": "3600 Burwood Dr",
      "address_2": "",
      "postal_code": "60085-8399",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of FL, IL, IN, MA, MS, NV, OH, TN, TX, WA.",
      "recall_number": "Z-0937-2023",
      "product_description": "HCT 50mL EVA BAGS, 2 Port, Sterile, Tripple Packaged, 20 EVA BAGS/Pack, 7 Packs PER CASE.  Distributed by Health Care Technology.",
      "product_quantity": "2,779 units",
      "reason_for_recall": "Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.",
      "recall_initiation_date": "20221215",
      "center_classification_date": "20230111",
      "report_date": "20230118",
      "code_info": "Assembly Number HCT2050, UDI-DI: M752HCT20502, Lot Number: 220130152, 221677841",
      "more_code_info": ""
    }
  ]
}