{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "86385",
      "product_res_number": "Z-0822-2010",
      "event_date_initiated": "2009-01-21",
      "event_date_posted": "2010-02-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-09-21",
      "res_event_number": "53702",
      "product_code": "KIR",
      "product_description": "Rabbit Kidney Culture, brand name:  'FreshCells'.  The product is labeled as 'Rabbit Kidney' also known as 'Rbk' , 2-square cm area of a cell monolayer covered with 2-mL culture medium.  The product is packed in glass culture tubes 16x125mm, with screw caps.  The product is distributed in EPS shipping racks which can hold up to 50 tubes each.\n\nUsed routinely for in vitro diagnostic testing for virus and/or Chlamydia isolation and to aid in the diagnosis of diseases associated with infectious agents.",
      "code_info": "Catalog Number:  48-0600, Lot #480109.",
      "firm_fei_number": "1000122536",
      "recalling_firm": "Diagnostic Hybrids Inc",
      "address_1": "1055 East State Street",
      "address_2": "Suite 100",
      "city": "Athens",
      "state": "OH",
      "postal_code": "45701-1526",
      "additional_info_contact": "740-589-3300",
      "reason_for_recall": "During QC post release monitoring, the firm determined that the monolayer culture of rabbit kidney cells previously distributed by the firm, appeared to contain another type of cells (monkey kidney cells).",
      "root_cause_description": "Process control",
      "action": "Diagnostic Hybrids issued a \"Product Notification\" letter dated January 23, 2009 in addition to verbal communication of the affected product beginning January 21, 2009.  The firm requested that all affected product be discarded /destroyed and not use for diagnostic testing.  Consignees were asked to complete and return a Fax-Back form.\n\nFor further information, contact Diagnostic Hybrids Technical Services at 1-866-344-3477 or 1-740-589-3300.",
      "product_quantity": "1127 units",
      "distribution_pattern": "Worldwide Distribution -- United States (CA, FL, GA, MA, MO, NY, NJ, TN, TX and VA),  Ontario Canada and Manitoba Canada.",
      "openfda": {
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        ],
        "device_name": "Cells, Animal And Human, Cultured",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.2280",
        "device_class": "1",
        "registration_number": [
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