{
  "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": "Doral",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97419",
      "recalling_firm": "Quest International, Inc.",
      "address_1": "8127 Nw 29th St",
      "address_2": "N/A",
      "postal_code": "33122-1051",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of Utah, Texas, and Arizona.",
      "recall_number": "Z-2552-2025",
      "product_description": "Brand Name: ReQuest Measles IgM  Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM  Model/Catalog Number: 01-190M  Software Version: N/A  Product Description: Measles IgM tests, performed using ELISA (Enzyme-Linked Immunosorbent Assay) method, used to detect the presence of IgM antibodies against measles virus in a patient's serum or plasma  Component: not a component",
      "product_quantity": "376 kits",
      "reason_for_recall": "Measles IgM Test Kit lacks  premarket approval or clearance.",
      "recall_initiation_date": "20250717",
      "center_classification_date": "20250911",
      "report_date": "20250917",
      "code_info": "UDI I# 00850487007104 -  Lots affected: G00024; K04024; M11024; M12024; D01025; E04025,F04025"
    }
  ]
}