{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "189595",
      "product_res_number": "Z-0179-2022",
      "event_date_initiated": "2021-09-27",
      "event_date_posted": "2021-10-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-05-04",
      "res_event_number": "88805",
      "product_description": "BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton.\nUsed to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe.\n\nCatalog Number: 305822",
      "code_info": "Lot Number: 1111347\nExp. Date: 4/30/2026\nUDI: 10382903058225",
      "firm_fei_number": "2243072",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "city": "Franklin Lakes",
      "state": "NJ",
      "postal_code": "07417-1815",
      "additional_info_contact": "SAME\n201-847-6800",
      "reason_for_recall": "Holes in product packaging impacts package integrity and may compromise sterility.",
      "root_cause_description": "Equipment maintenance",
      "action": "BD notified consignees Urgent Medical DevIce Recall Letter dated 9/7/21  via FedEx and may also be contacted via e-mail (when available). Letter states reason for recall, health risk and action to take:\n1. Immediately review your inventory for the specific Catalog (Ref) and Lot number listed above. Destroy all product subject to the recall following your institution s process for destruction.\n2. Share this recall notification with all users within your facility network of the product to ensure they are also aware of this recall.\n3. Complete the attached Customer Response Form and return to the BD contact noted on the form whether or not you have any of the impacted material so that BD may acknowledge your receipt of this notification per FDA requirements and subsequently process any applicable product replacement.\n4. Report any adverse health consequences experienced with the use of this product to BD.\nBD will provide replacement product for all discarded inventory.\nContact Information: If you require further assistance, please contact:\nBD Contact Contact Information\nNorth American Regional Complaint Center\n1-84BD-LIFE (1-844-823-5433)\nSay  Recall  when prompted\nMon Fri 8:00am and 5:00pm CT",
      "product_quantity": "8,000 units",
      "distribution_pattern": "TX",
      "openfda": {}
    }
  ]
}