{
  "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": "2026-09-10",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "188134",
      "product_res_number": "Z-2452-2021",
      "event_date_initiated": "2021-03-01",
      "event_date_created": "2021-09-13",
      "recall_status": "Open, Classified",
      "res_event_number": "88206",
      "product_code": "QKP",
      "product_description": "Cellex qSARS-Cov-2 Antigen Rapid Test, 25 tests/box, submitted as EUA202955 \"declined to issue\"",
      "code_info": "All lot numbers",
      "firm_fei_number": "3014277758",
      "recalling_firm": "Cellex",
      "address_1": "507 Airport Blvd Ste 107 507 Airport Blvd",
      "address_2": "Ste 107",
      "city": "Morrisville",
      "state": "NC",
      "postal_code": "27560-8200",
      "reason_for_recall": "The kit does not have an emergency use authorization (EUA).",
      "root_cause_description": "Under Investigation by firm",
      "action": "The recall was initiated via phone.  The date the telephone calls were made is unknown but may have occurred late February, early March, 2021, based on the date returns started being made to the recalling firm.   The firm issued their initial letters dated 6/15/2021 via email as a result of not having documentation of the phone calls.  Later notifications were also issued or verbally discussed, with the latest notification occurring 8/20/2021.",
      "product_quantity": "Approximately 44,821 kits",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, TX, and WI.",
      "openfda": {
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        ],
        "device_name": "Coronavirus Antigen Detection Test System.",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}