{
  "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-0043-2020",
      "product_description": "Online TDM Vancomycin Gen.3 ( 200 tests)  Catalog # 06779344190  Analyzer/Module: cobas c 311 and cobas c 501/502",
      "product_quantity": "33979 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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}