{
  "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": "2026-08-20",
    "results": {
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  "results": [
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      "cfres_id": "167606",
      "product_res_number": "Z-0389-2019",
      "event_date_initiated": "2018-08-10",
      "event_date_created": "2018-11-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2019-12-04",
      "res_event_number": "81160",
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      "code_info": "Lot Number 808801-180;  UDI: 00811727011411",
      "firm_fei_number": "1827821",
      "recalling_firm": "Medtest Holdings, Inc.",
      "address_1": "5449 Research Dr",
      "city": "Canton",
      "state": "MI",
      "postal_code": "48188-2261",
      "additional_info_contact": "Diane Zalac\n734-487-8300 Ext. 144",
      "reason_for_recall": "Vials of the autoHDL/LDL Calibrator were shipped without a vial label.",
      "root_cause_description": "Error in labeling",
      "action": "Notification letters dated 8/14/18 were sent to customers.  Customers were also contacted via telephone on 8/10/18.  Additional letters containing labels dated 8/17/18 were sent to customers.",
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