{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hauppauge",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93546",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0592-2024",
      "product_description": "Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE",
      "product_quantity": "705",
      "reason_for_recall": "Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance level (SAL) of 10^-6 cannot be guaranteed. Risks to patients if product is used include blood stream infections, urinary tract infections, or respiratory infections; in the worst-case scenario, there is risk of sepsis or death.",
      "recall_initiation_date": "20231130",
      "center_classification_date": "20240103",
      "report_date": "20240110",
      "code_info": "UDI-DI 00849233010000 Lots 2210099 2210135 2210337 2210377 2310181 2310233 2310291"
    }
  ]
}