{
  "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": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85432",
      "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": "E-Mail",
      "distribution_pattern": "Nationwide domestic distribution. Foreign distribution to Austria, Belgium, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, UK, Australia, Canada, Mexico, Malaysia, New Zealand",
      "recall_number": "Z-2065-2020",
      "product_description": "BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535",
      "product_quantity": "16,099,310 units",
      "reason_for_recall": "This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.",
      "recall_initiation_date": "20200416",
      "center_classification_date": "20200520",
      "termination_date": "20210901",
      "report_date": "20200527",
      "code_info": "Lots 8353952  9011582  9017875  9024676  9045702  9060999  9079716  9127571  9143529  9156595  9163601"
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