{
  "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": "Des Plaines",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93902",
      "recalling_firm": "Abbott Molecular, Inc.",
      "address_1": "1300 E Touhy Ave",
      "address_2": "",
      "postal_code": "60018-3315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, IL, MA, MD, MN, NY, and PA.",
      "recall_number": "Z-1188-2024",
      "product_description": "In-vitro diagnostic kits:    (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit, REF 01N15-010;  (2) Abbott Vysis LSI D13S319 (13q14.3) SpectrumOrange Probe, REF 01N34-020;",
      "product_quantity": "16 kits",
      "reason_for_recall": "Products that were intended for export only which were not approved or registered in accordance with U.S. specifications were shipped to U.S. customers.",
      "recall_initiation_date": "20240201",
      "center_classification_date": "20240226",
      "report_date": "20240306",
      "code_info": "(1) REF 01N15-010 - GTIN 00884999035362, Lot #381146, Exp. 2024-05-05; #381870, Exp. 2024-05-05; #382179 Exp. 2024-05-05; #387021, Exp. 2024-08-01; #528081, exp. 2023-11-16;   (2) REF 01N34-020 - GTIN 00884999000766, Lot #522756, Exp. 2023-06-21.",
      "more_code_info": ""
    }
  ]
}