FDAAugust 2, 2021device

Flow sensors that may be installed in the following GEHC anesthesia machines: (1) Aestiva MRI, GTIN 0080682102339; (2) Aestiva 7900; (3) Aestiva 7100; (4) Aespire System Carestation, S/5 Protiva Config., Aespire 100 Compact Wall Mount (Aespire 7100); (5) S/5 Aespire 7900; (6) Aespire View; (7) Av...

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

The hazard

The flow sensors built prior to June 2021 could have damaged tubes with small punctures or cuts that could cause leaks resulting in incorrect anesthesia machine tidal volumes potentially leading to over-delivery of volume to the patient.

What to do

FDA enforcement status: Ongoing

Brands named

ge healthcare

UPCs

00806821023390084068210229200840682102322

Recall history

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

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