{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "The affected lots may exhibit inaccuracy for Quality Control and patient samples at the low end of the Analytical Measurement Range. The bias is due to the calibration curve not showing separation between the Level 1 and Level 2 calibrators.",
      "address_2": "Po Box 6101",
      "product_quantity": "7543",
      "code_info": "Lots EB8115  BB8159  FB8275",
      "center_classification_date": "20180613",
      "distribution_pattern": "Nationwide distribution. Foreign distribution to Argentina, Australia, Brazil, Bahamas, Canada, Germany, India, Japan, Myanmar, New Zealand, Saudi Arabia, Taiwan, and South Africa.",
      "state": "DE",
      "product_description": "Dimension Gentamicin Flex reagent cartridge, DM GENT,  gentamicin enzyme immunoassay, Lot numbers affected are EB8115, BB8159, and FB8275.",
      "report_date": "20180620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-2181-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80009",
      "termination_date": "20200424",
      "recall_initiation_date": "20180419",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}