{
  "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": [
    {
      "country": "United States",
      "city": "Indianapolis",
      "address_1": "9115 Hague Rd",
      "reason_for_recall": "Homocysteine Reagent, Calibration Failures and  Quality Control Recovery Issues on cobas c 701 and 702 modules",
      "address_2": "",
      "product_quantity": "82 units (US)",
      "code_info": "Lot Number: 422313   Exp Date:  07/31/2020",
      "center_classification_date": "20191213",
      "distribution_pattern": "US Nationwide distribution in the states of NJ, HI, IA.",
      "state": "IN",
      "product_description": "Roche Homocysteine-In vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c systems   Catalog  Number: 06542921190 - - Product Usage: The assay can assist in the diagnosis of patients suspected of having hyperhomocysteinemia or homocystinuria.",
      "report_date": "20191225",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "recall_number": "Z-0679-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84018",
      "termination_date": "20201009",
      "more_code_info": "",
      "recall_initiation_date": "20191004",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}