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FDAApril 2, 2015device

FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalation anesthesia on neonatal to adult patient populations.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

In some Flow-i Anesthesia Systems, patient cassette can get dislodged which could result in gas leakage within the system internal circuit potentially leading to a stop in ventilation.

What to do

FDA enforcement status: Terminated

Brands named

maquet cardiovascular us salesmaquetmaquet cardiovascular

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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