{
  "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": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "BD has  received multiple reports of units associated with the 23 G x .75 in. BD Vacutainer¿ Push Button Blood  Collection Set with 12 in. Tubing whose lots are exhibiting separation of  front and rear barrels upon activation of the safety feature, which retracts the  needle.",
      "address_2": "",
      "product_quantity": "1,788,150 units",
      "code_info": "5355531  5355533  5356681  5356682  6006629  6006630  6006631  6006633  6006634  6006650",
      "center_classification_date": "20161212",
      "distribution_pattern": "Worldwide distribution- US (nationwide) and countries of: Canada, Belgium, Brazil.",
      "state": "NJ",
      "product_description": "BD 23 G x .75 in. BD Vacutainer¿ Push Button Blood  Collection Set with 12 in. Tubing    Catalog # 367342    Intended for venipuncture to obtain blood specimens from patients.",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-0745-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75252",
      "more_code_info": "",
      "recall_initiation_date": "20160808",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}