{
  "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": "Ashland",
      "address_1": "28 Howe St",
      "reason_for_recall": "The Overpressure Safety Valve is not cleared with an indication for use on the arterial side of the extracoporeal bypass circuit. It is intended for use only on the venous side. There is a remote possibility of minimal blood loss, fluid weeping, or dripping on the user.",
      "address_2": "",
      "product_quantity": "163 devices",
      "code_info": "Part Number: 66086-01: Lot Numbers: RG09, RM20 and Part Number: 70700-03: Lot Numbers: QL09, RH07, RL15, QG17, RD03",
      "center_classification_date": "20150622",
      "distribution_pattern": "Distributed to the states of MO and FL.",
      "state": "MA",
      "product_description": "Custom Cardiovascular Procedure Kits; Over-Pressure Safety Valves.    For use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it.",
      "report_date": "20150701",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Cardiovascular Systems Corp",
      "recall_number": "Z-1828-2015",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "71196",
      "termination_date": "20150727",
      "more_code_info": "",
      "recall_initiation_date": "20150506",
      "postal_code": "01721-1305",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}