{
  "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": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93849",
      "recalling_firm": "Maquet Medical Systems USA",
      "address_1": "45 Barbour Pond Dr",
      "address_2": "N/A",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution.",
      "recall_number": "Z-1076-2024",
      "product_description": "Model No. BEQ-HLS 5050 USA,  HLS Set Advanced 5.0, Product Code/Part Number 70106.9077.  Used with the CARDIOHELP heart-lung machine.",
      "product_quantity": "16520 worldwide; 6657 US",
      "reason_for_recall": "The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.",
      "recall_initiation_date": "20240116",
      "center_classification_date": "20240213",
      "report_date": "20240221",
      "code_info": "UDI-DI 04058863076355 Lots 3000301222, 3000319782, 3000327602  ***Added 3/21/24*** 3000333098, 3000352360, 3000357174"
    }
  ]
}