{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "West Sacramento",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65188",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "2040 Enterprise Blvd",
      "address_2": "N/A",
      "postal_code": "95691-3427",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1525-2013",
      "product_description": "Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels (B1017-417), SMN #: 10483099),     For use in determining quantitative and/or qualitative antimicrobial agent susceptibility.",
      "product_quantity": "683 units",
      "reason_for_recall": "The product has the potential for false negative or delayed reaction for Arginine (ARG) results. In addition, 42 hour identification panel holds may occur due to a weak ARG reaction.",
      "recall_initiation_date": "20130502",
      "center_classification_date": "20130608",
      "termination_date": "20130917",
      "report_date": "20130619",
      "code_info": "Lot: 2013-11-13, Exp 11/13/2013."
    }
  ]
}