{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Branchburg",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73703",
      "recalling_firm": "Roche Molecular Systems, Inc.",
      "address_1": "1080 US Highway 202 S",
      "address_2": "N/A",
      "postal_code": "08876-3733",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Hungary",
      "recall_number": "Z-1830-2016",
      "product_description": "cobas¿ EGFR Mutation Test, v2 and cobas¿ cfDNA Sample  Preparation Hungarian Translation Instructions for Use",
      "product_quantity": "8 kits",
      "reason_for_recall": "An error was found within the Hungarian translations of the cobas¿ EGFR Mutation Test v2 Instructions for Use (M/N  07340761001-01HU, Doc Rev. 1.0, Dated 08/2015) and the cobas¿ cfDNA Sample Preparation Kit Instructions for Use  (M/N 07573758001-01HU, Doc. Rev. 1.0, Dated 05/2015).",
      "recall_initiation_date": "20160315",
      "center_classification_date": "20160526",
      "termination_date": "20171211",
      "report_date": "20160601",
      "code_info": "EGFR v2: 07248563190  cfDNA: 07247737190"
    }
  ]
}