{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "177220",
      "product_res_number": "Z-0500-2020",
      "event_date_initiated": "2019-10-14",
      "event_date_created": "2019-11-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-10-16",
      "res_event_number": "84113",
      "product_code": "NGT",
      "k_numbers": [
        "K161552"
      ],
      "product_description": "BD Posiflush Pre-Filled Normal Saline Syringes\nCatalog Number: 306575 (Canada only)",
      "code_info": "Lot Number: 9175971 UDI: 50382903065757",
      "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": "888-731-7973",
      "reason_for_recall": "Limited number of syringes labeled  Posiflush Experimental Product  and  Not for Human Use  being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.",
      "root_cause_description": "Packaging process control",
      "action": "BD issued notifications to Customers via FedEx to Distributors, Pharmacies, and Consumers via Pharmacies on 10/14/19, advising of the problem, health risk and action to take: Immediately review your inventory for the specific Catalog and Lot number listed , discontinue use and destroy all product subject to the recall following your institutions process for destruction.2. Complete the Customer Recall Response Form. Questions or require further assistance, please contact 1-888-731-7973 between 8 AM and 5 PM ET Monday through Friday.",
      "product_quantity": "967,680",
      "distribution_pattern": "Distribution US Nationwide and Canada",
      "openfda": {
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        "device_name": "Saline, Vascular Access Flush",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5200",
        "device_class": "2"
      }
    }
  ]
}