{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Milano",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72311",
      "recalling_firm": "Sentinel CH SpA",
      "address_1": "Via Robert Koch 2",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-0164-2016",
      "product_description": "Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.",
      "product_quantity": "765 kits",
      "reason_for_recall": "Results for ammonia are below the linear range of the assay for samples that have been collected in sodium or lithium heparin tubes.",
      "recall_initiation_date": "20150922",
      "center_classification_date": "20151026",
      "termination_date": "20160330",
      "report_date": "20151104",
      "code_info": "Lot 50083Y600, expiration date 31 Jul 2016."
    }
  ]
}