{
  "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": "2026-07-22",
    "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": "99259",
      "recalling_firm": "Maquet Cardiovascular, LLC",
      "address_1": "45 Barbour Pond Dr",
      "address_2": "",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of NY, CA, SC, FL, TX, GA, OR.",
      "recall_number": "Z-2741-2026",
      "product_description": "The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI  00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.",
      "product_quantity": "205 units",
      "reason_for_recall": "Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-28782A) performed by STERIS at its Whippany, NJ facility between March 31 and April 1 of 2026.",
      "recall_initiation_date": "20260602",
      "center_classification_date": "20260715",
      "report_date": "20260722",
      "code_info": "UDI 00607567700406, Serial/Lot Number 3000547797",
      "more_code_info": ""
    }
  ]
}