{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Raritan",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92017",
      "recalling_firm": "Ortho-Clinical Diagnostics, Inc.",
      "address_1": "1001 Us Highway 202",
      "address_2": "N/A",
      "postal_code": "08869-1424",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, AZ, CA,  GA, NY.",
      "recall_number": "Z-1396-2023",
      "product_description": "VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody  Calibrators programmed onto the Assay Data Disks (ADD) Data Release Versions (DRV):  DRVs 6213 through 6218 supporting VITROS Calibrators.  Product Code: 6199976",
      "product_quantity": "256 units",
      "reason_for_recall": "Incorrect Number of Calibrator Levels (2) Set for the VITROS Immunodiagnostics Products Anti-SARS-CoV-2 Total N Antibody Calibrators in Assay Data Disks (ADD),  resulting in delayed patients results",
      "recall_initiation_date": "20230309",
      "center_classification_date": "20230418",
      "report_date": "20230426",
      "code_info": "UDI: 10758750034581 Lot # /Expiration Date: 0230   22-Feb-2023; 0240   22-Mar-2023; 0250   26-Apr-2023."
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}