{
  "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": [
    {
      "country": "United States",
      "city": "Princeton",
      "address_1": "400 College Rd E",
      "reason_for_recall": "The i-STAT PT/INR cartridges have the potential to exhibit incorrectly elevated results.",
      "address_2": "",
      "product_quantity": "2,950,296 cartridges US; 156,408 cartridges OUS",
      "code_info": "List number  04J50-01  04J5O-02  03P89-24    Lots begininng with R11 or R12",
      "center_classification_date": "20120808",
      "distribution_pattern": "Worldwide Distribution -- (USA) nationwide",
      "state": "NJ",
      "product_description": "I-STAT PT/INR cartridge  Abbott Point of Care Inc.  Abbott Park, IL 60064 USA    This cartridge is useful for monitoring patients receiving oral anticoagulation therapy such as Coumadin or warfarin.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Point Of Care Inc.",
      "recall_number": "Z-2157-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62536",
      "termination_date": "20130208",
      "more_code_info": "",
      "recall_initiation_date": "20120301",
      "postal_code": "08540-6607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}