{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83467",
      "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": "Letter",
      "distribution_pattern": "AK  AL  AR  AZ  CA  CO  CT  DC  DE  FL  GA  GU  HI  IA  ID  IL  IN  KS  KY  LA  MA  MD  ME  MI  MN  MO  MS  MT  NC  ND  NE  NH  NJ  NM  NV  NY  OH  OK  OR  PA  PR  RI  SC  SD  TN  TX  UT  VA  VT  WA  WI  WV  WY",
      "recall_number": "Z-0042-2020",
      "product_description": "Online TDM Vancomycin Gen.3 (100 tests)  Catalog # 06779336190  Analyzer/Module: cobas c 311 and cobas c 501/502",
      "product_quantity": "27676 units",
      "reason_for_recall": "Inaccurately Low Sample Results",
      "recall_initiation_date": "20190723",
      "center_classification_date": "20191004",
      "termination_date": "20200608",
      "report_date": "20191016",
      "code_info": "All Lots"
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}