{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84113",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "address_2": "N/A",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US Nationwide and Canada",
      "recall_number": "Z-0499-2020",
      "product_description": "BD Posiflush Pre-Filled Normal Saline Syringes  Catalog Number: 306547",
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      "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.",
      "recall_initiation_date": "20191014",
      "center_classification_date": "20191120",
      "termination_date": "20201016",
      "report_date": "20191127",
      "code_info": "Lot Number: 9142881  UDI: 50382903065474"
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