{
  "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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  },
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      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82851",
      "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": "Nationwide  Foreign:  AR  AU  BE  BN  BR  CA  CL  CN  CO  CR  CW  EC  GT  GY  HK  HN  ID  IN  JP  KR  MX  MY  NI  NZ  PA  PE  PG  PH  PK  SG  SR  SV  TH  TW  UY  VN",
      "recall_number": "Z-0057-2020",
      "product_description": "BD MicrotainerTubes with K2E (K2EDTA)  Catalog Number: 365974",
      "product_quantity": "N/A",
      "reason_for_recall": "Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.",
      "recall_initiation_date": "20190513",
      "center_classification_date": "20191007",
      "termination_date": "20200806",
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