{
  "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": "Newark",
      "state": "DE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79468",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "500 Gbc Dr Ms 514",
      "address_2": "Po Box 6101",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic and Foreign consignees",
      "recall_number": "Z-1796-2018",
      "product_description": "Dimension Lipase Flex¿ Reagent Cartridge -  ( Lipase-esterase, enzymatic, photometric, lipase)",
      "product_quantity": "N/A",
      "reason_for_recall": "Calibration failure - confirmed a positive bias with LIPL lot FB8109 when compared to other Dimension LIPL lots. Lot FB8109 is not meeting Siemens internal specifications for lot-to-lot limits.",
      "recall_initiation_date": "20171214",
      "center_classification_date": "20180510",
      "termination_date": "20201203",
      "report_date": "20180516",
      "code_info": "Catalog DF56  Lot FB8109- UDI# (01)00842768025532(10)FB8109(17)20180419"
    }
  ]
}