{
  "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": "89965",
      "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": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0953-2022",
      "product_description": "Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02",
      "product_quantity": "12,632 kits",
      "reason_for_recall": "Point of Care (PoC) rapid test products were distributed to customers who did not have a valid CLIA ID.",
      "recall_initiation_date": "20220401",
      "center_classification_date": "20220427",
      "termination_date": "20240611",
      "report_date": "20220504",
      "code_info": "All lots distributed to end users without valid CLIA ID   UPC: 8 806121 763044   Distributed from December 2021 through February 2022.",
      "more_code_info": ""
    }
  ]
}