{
  "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,
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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-0325-2023",
      "product_description": "Busse JOINT INJECTION TRAY -Intended as a nerve block   REF No. 8561 R1",
      "product_quantity": "80 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)00849233016712 Lot Number: 2230276",
      "more_code_info": ""
    }
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}