{
  "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": "Hauppauge",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90072",
      "recalling_firm": "Busse Hospital Disposables, Inc.",
      "address_1": "75 Arkay Dr",
      "address_2": "N/A",
      "postal_code": "11788-3707",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1157-2022",
      "product_description": "I.V. Start Kit  \t  Catalog 8172",
      "product_quantity": "4218 units",
      "reason_for_recall": "Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products",
      "recall_initiation_date": "20220222",
      "center_classification_date": "20220528",
      "termination_date": "20240417",
      "report_date": "20220608",
      "code_info": "Lot Numbers: 2020561 2020560 2020650 2120089 2120018 2120344 2120442 2120645 2120768 2120911  UDI: 00849233015883"
    }
  ]
}