{
  "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": "89216",
      "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": "Letter",
      "distribution_pattern": "Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA.  There was no foreign/military/government distribution.",
      "recall_number": "Z-0502-2022",
      "product_description": "greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P",
      "product_quantity": "889,200 pcs.",
      "reason_for_recall": "Some of the blood collection tubes show clotting due to variation of Lithium Heparin.",
      "recall_initiation_date": "20211209",
      "center_classification_date": "20220118",
      "termination_date": "20231010",
      "report_date": "20220126",
      "code_info": "Lot #B21053QG, Exp. 09/09/2022, UDI:  Case: 39120017579046, Rack: 29120017579049."
    }
  ]
}