{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Elkton",
      "address_1": "125 Blue Ball Rd",
      "reason_for_recall": "Sterility of medical devices intended for use in surgical procedures may be compromised.",
      "address_2": "",
      "product_quantity": "26 units",
      "code_info": "Lot numbers: 21K, 31K, 32K, 33K, 34K, 35K",
      "center_classification_date": "20140221",
      "distribution_pattern": "USA Nationwide Distribution in the state of LA, NJ, and NY.",
      "state": "MD",
      "product_description": "VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System, Part number: VSP550, Sterile***Rx Only***    Product Usage:  The VirtuoSaph \u001c Plus Endoscopic Vessel Harvesting System is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass.",
      "report_date": "20140305",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "recall_number": "Z-1069-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67193",
      "termination_date": "20150728",
      "more_code_info": "",
      "recall_initiation_date": "20131212",
      "postal_code": "21921-5315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}