{
  "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": "Monroe",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88511",
      "recalling_firm": "Greiner Bio-One North America, Inc.",
      "address_1": "4238 Capital Dr",
      "address_2": "N/A",
      "postal_code": "28110-7681",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Distribution was made to AL, AZ, CO, CT, FL, IL, MA, MD, MI, MO, NC, NM, PA, TX, and VA.  Foreign distribution was made to Canada.",
      "recall_number": "Z-2485-2021",
      "product_description": "VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged",
      "product_quantity": "962,400 tubes",
      "reason_for_recall": "Blood collection tubes may experience a clotting issue.",
      "recall_initiation_date": "20210813",
      "center_classification_date": "20210924",
      "termination_date": "20230816",
      "report_date": "20211006",
      "code_info": "Item Number 456279, Lot B21033DA, exp. 09/08/2022, UDI Case - 39120017571248; UDI Rack - 29120017571241  UPDATE per 9/10/2021 email:  Item Number 456279, Lot B21053R8, exp. 11/10/2022, UDI Case -39120017571248; UDI Rack - 29120017571241."
    }
  ]
}