{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86897",
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Domestic: IL, FL, GA, WV",
      "recall_number": "Z-0752-2021",
      "product_description": "cobas pro integrated solutions -cobas c 503, Analyzer, chemistry (photometric discrete), for clinical use",
      "product_quantity": "152 kits and 7 units",
      "reason_for_recall": "During the subsequent pipetting (1st or 2nd  measurement), the residual reagent can sporadically be transferred from the conus into the reaction cuvette and lead to inaccurately low results for the affected TDMs (Therapeutic Drug Monitoring).",
      "recall_initiation_date": "20201123",
      "center_classification_date": "20201229",
      "termination_date": "20230706",
      "report_date": "20210106",
      "code_info": "Catalog Number  08445605190  08445567190  08253153190  08058580190"
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}