{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sparks",
      "address_1": "BD Diagnostic Systems",
      "reason_for_recall": "The products may exhibit indications of excessive oxidation.  Excessive oxidation may affect the viability of anaerobic microorganisms.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "145,860 tubes",
      "code_info": "Part/Cat No.     Lot / Serial   No.Date of Mfr Exp. Date    221606      4042455       2/25/2014 2/5/2015  221606      4067180       3/18/2014 3/5/2015  221606      4087204       4/10/2014 3/25/2015  221606      4124702       5/8/2014 4/24/2015  221606      4161968       7/7/2014 6/12/2015  221606      4181959       7/14/2014 7/3/2015  221606             4032407       2/14/2014                  1/29/2015  221606             4042069       2/17/2014                   2/4/2015",
      "center_classification_date": "20150610",
      "distribution_pattern": "US Nationwide distribution  in AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NV, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY.",
      "state": "MD",
      "product_description": "BBL Port A Cul tubes, catalog number 221606.  Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport medium and are intended to maintain the viability of anaerobic, facultative and aerobic microorganisms during transport from the patient to the laboratory. Sterile packages are for collection of specimens in clean areas; e.g., surgical suites.",
      "report_date": "20150617",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-1746-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "69954",
      "termination_date": "20160107",
      "recall_initiation_date": "20141121",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}