{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97443",
      "recalling_firm": "Abbott Point Of Care Inc.",
      "address_1": "400 College Rd E",
      "address_2": "N/A",
      "postal_code": "08540-6607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2583-2025",
      "product_description": "i-STAT CG8+ cartridge. List Number: 03P88-25.      510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300",
      "product_quantity": "8,962,450  units",
      "reason_for_recall": "Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.",
      "recall_initiation_date": "20250821",
      "center_classification_date": "20250917",
      "report_date": "20250924",
      "code_info": "List Number: 03P88-25. All lot numbers."
    }
  ]
}