{
  "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": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "Non-Conforming devices were shipped from the service center without proper evaluation and therefore may be nonconforming.",
      "address_2": "",
      "product_quantity": "2",
      "code_info": "Model 1100-9034-000 Mfg. Lot or Serial # BGBQ00675 and BGBQ01187",
      "center_classification_date": "20180326",
      "distribution_pattern": "US Distribution to states of: AZ, IL NC, NH and PA.",
      "state": "WI",
      "product_description": "DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE     Cassettes are intended to be used to deliver anesthetic agent.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-1199-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79493",
      "termination_date": "20200410",
      "more_code_info": "",
      "recall_initiation_date": "20171004",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}