{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
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  "results": [
    {
      "cfres_id": "204219",
      "product_res_number": "Z-0314-2024",
      "event_date_initiated": "2023-11-01",
      "event_date_posted": "2023-11-16",
      "recall_status": "Open, Classified",
      "res_event_number": "93379",
      "product_code": "OIB",
      "product_description": "BLOOD CULTURE KIT, REF DYNDH1647B",
      "code_info": "UDI/DI 40195327267002 (case), 10195327267001 (unit):  Lot Numbers: 23CMH028, 23CMD954",
      "firm_fei_number": "1417592",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "city": "Northfield",
      "state": "IL",
      "postal_code": "60093-2753",
      "additional_info_contact": "Karin Johnson\n886-359-1704",
      "reason_for_recall": "This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Medline Industries issued a MEDICAL DEVICE RECALL notice to its consignees on 11/01/2023 via email.  The notice explained the issue and requested that the destruction of the affected kits.  Consignees were also instructed to  notify all parties if the kits were transferred.",
      "product_quantity": "1890 kits",
      "distribution_pattern": "US Nationwide distribution in the state of California.",
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        "device_name": "Blood And Urine Collection Kit (Excludes Hiv Testing)",
        "medical_specialty_description": "Pathology",
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}