{
  "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": "Princeton",
      "address_1": "400 College Rd E",
      "reason_for_recall": "Inaccurate potassium results may be generated. When testing with control fluid and/or patient samples with low or reference range potassium concentration, elevated potassium results may be generated. When testing with samples with a high concentration of potassium, decreased potassium results may be generated",
      "address_2": "",
      "product_quantity": "17550 cartridges",
      "code_info": "Lot Number: L18059  Box Numbers:  0221, 0222, 0223, 0224, 0231, 0232, 0233",
      "center_classification_date": "20181214",
      "distribution_pattern": "WI",
      "state": "NJ",
      "product_description": "Abbott i-STAT CG8+ Cartridges intended for use in the in vitro quantification of potassium in arterial, venous, or capillary whole blood.   List Number/UDI# : 03P88-25 ,(01)10054749000163(17)181028(10)L18059",
      "report_date": "20181226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Point Of Care Inc.",
      "recall_number": "Z-0615-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81151",
      "termination_date": "20190404",
      "more_code_info": "",
      "recall_initiation_date": "20180913",
      "postal_code": "08540-6607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}