{
  "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": "2026-08-27",
    "results": {
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  "results": [
    {
      "cfres_id": "151129",
      "product_res_number": "Z-0895-2017",
      "event_date_initiated": "2016-11-15",
      "event_date_created": "2016-12-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-06-21",
      "res_event_number": "75746",
      "product_code": "FCH",
      "product_description": "BREAST PACK, Surgical Instrument Tray, REF/Catalog No. 5406, STERILE, Rx Only -- busse Hospital Disposables Hauppauge, NY --- Device Listing # E193298.",
      "code_info": "Lot Number 1230323, Exp. Date December 2016;  Lot Number 1230387, Exp. Date December 2016;  Lot Number 1231616, Exp. Date December 2016",
      "firm_fei_number": "2433012",
      "recalling_firm": "Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables",
      "address_1": "75 Arkay Dr",
      "city": "Hauppauge",
      "state": "NY",
      "postal_code": "11788-3707",
      "additional_info_contact": "Muhamad Ansari\n631-435-4711 Ext. 254",
      "reason_for_recall": "Covidien issued a labeling update for the Covidien Devon Light Gloves.  Busse had incorporated the affected gloves in several kits and distributed them prior to receipt of the recall notification.",
      "root_cause_description": "Other",
      "action": "Busse Hospital Disposables sent a Medical Device Correction letter (dated November 11, 2016) and response form to the three customers via FedEx on 11/15/2016 to inform them of the recall of the kits containing the affected gloves.  This was done without notifying NYK-DO.",
      "product_quantity": "US: 35 cases",
      "distribution_pattern": "PA, FL, VA",
      "openfda": {
        "device_name": "Tray, Biopsy, Without Biopsy Instruments",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4730",
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        "k_number": [
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}