{
  "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": "Ongoing",
      "city": "Germantown",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89914",
      "recalling_firm": "Qiagen Sciences LLC",
      "address_1": "19300 Germantown Rd",
      "address_2": "",
      "postal_code": "20874-1415",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "AZ  CA  CT  FL  GA  IL  IN  MA  MN  NC  NY  OK  OR  PA  TN  TX  WV",
      "recall_number": "Z-0952-2022",
      "product_description": "therascreen KRAS RGQ PCR Kit (24)  REF 874052 (Japan IVD, not released in the USA)",
      "product_quantity": "8 Kits",
      "reason_for_recall": "False positive or false negative G12C (12CYS) mutation result for the KRAS Mutation Status resulting from Flags/Warnings may invalidate the result for one or more individual mutation target of the kit.",
      "recall_initiation_date": "20220225",
      "center_classification_date": "20220418",
      "report_date": "20220427",
      "code_info": "All lot numbers",
      "more_code_info": ""
    }
  ]
}