{
  "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": "Jersey City",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89516",
      "recalling_firm": "CELLTRION USA INC",
      "address_1": "1 Evertrust Plz Ste 1207",
      "address_2": "",
      "postal_code": "07302-3087",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to TX.",
      "recall_number": "Z-0680-2022",
      "product_description": "Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02",
      "product_quantity": "8080 kits originally distributed; 726 kits redistributed",
      "reason_for_recall": "Returned test kits were erroneously shipped to customers. The kits are intended for Research Use Only (RUO). Additional RUO test kits were shipped to customers unlikely to use them for RUO purposes, and the firm provided a letter assuring distributors that RUO tests could be used for clinical diagnosis.",
      "recall_initiation_date": "20211202",
      "center_classification_date": "20220302",
      "termination_date": "20240610",
      "report_date": "20220309",
      "code_info": "Lots COVGCCF0001, COVGCCF0002",
      "more_code_info": ""
    }
  ]
}