{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82351",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "address_2": "",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan.",
      "recall_number": "Z-0252-2020",
      "product_description": "BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608",
      "product_quantity": "2,624,160 (2,169,703 US; 454,457 OUS)",
      "reason_for_recall": "BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.",
      "recall_initiation_date": "20190307",
      "center_classification_date": "20191031",
      "termination_date": "20220211",
      "report_date": "20191106",
      "code_info": "Lot 8207894  ***UPDATED 7/11/19***  Lots 9025826 and 8354527  ***UPDATED 12/10/19***  Lot 9010765",
      "more_code_info": ""
    }
  ]
}