{
  "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": [
    {
      "status": "Terminated",
      "city": "Rochester",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85762",
      "recalling_firm": "Ortho Clinical Diagnostics",
      "address_1": "100 Indigo Creek Dr",
      "address_2": "N/A",
      "postal_code": "14626-5101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution  Foreign:  Country  AR  AU  BR  CA  CL  CN  CO  DO  FR  ID  IN  JP  KR  MX  MY  NP  PE  PH  SG  TH  TT  VE  VN",
      "recall_number": "Z-2480-2020",
      "product_description": "VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below  Product Code: 6802783, Unique Identifier: 10758750002979",
      "product_quantity": "779  (U.S.= 225;OUS= 554)",
      "reason_for_recall": "Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be inadvertently reset to default in certain circumstances",
      "recall_initiation_date": "20200520",
      "center_classification_date": "20200701",
      "termination_date": "20221116",
      "report_date": "20200708",
      "code_info": "Affected Serial Number Range:  J36000109-J36001317"
    }
  ]
}