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Recall Observatory FDA recall evidence

Device product

CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal bypass circuit for circulatory and/or pulmonary support for periods appropriate to cardiopulmonary bypass (up to six hours). Product REF Numbers: 701072780; 701048012

Z-0595-2024

November 14, 2023

Class III

Product summary

Firm
Maquet Medical Systems USA
Event
Event 93462
Status
Ongoing
Classification
Class III
Quantity
1594 units
Official record key
device-enforcement:Z-0595-2024

Official wording

Reason: CARDIOHELP-i System was not properly tested to measure leakage current

Code information: UDI-DI: 04058863074863; 04037691658384 All serial numbers up to and including 90415172

Distribution pattern: Nationwide-WW Distribution to Argentina, Australia, Austria, Azerbaijan, Bahrain, Belgium, Brazil, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, French Polynesia, Germany, Ghana, Greece, Hong Kong, Iceland, India, Iran, Islamic Republic Of, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic Of Kuwait, Lebanon, Luxembourg, Macao, Maldives, Martinique, Mayotte, Mexico, Netherlands, New Zealand, Norway, Oman, Pakistan, Paraguay, Peru, Philippines, Poland, Portugal, Puerto Rico, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom,Vietnam, Yemen

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    CARDIOHELP-i System was not properly tested to measure leakage current