{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Hauppauge",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91079",
      "recalling_firm": "Busse Hospital Disposables, Inc.",
      "address_1": "75 Arkay Dr",
      "address_2": "",
      "postal_code": "11788-3707",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "TX",
      "recall_number": "Z-0326-2023",
      "product_description": "Busse SPINE INJECTION TRAY-Intended as a nerve block  REF No. 8563R1",
      "product_quantity": "40 cases",
      "reason_for_recall": "Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable",
      "recall_initiation_date": "20221021",
      "center_classification_date": "20221129",
      "report_date": "20221207",
      "code_info": "UDI-DI: (01) 00849233016705 Lot Number: 2230458",
      "more_code_info": ""
    }
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}