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FDAMay 19, 2023device

TruSignal Ear Sensor, REF TS-E-D; Oximeter

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

The hazard

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

What to do

FDA enforcement status: Ongoing

Brands named

ge healthcare finland oy

UPCs

00840682103251

Recall history

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

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TruSignal Ear Sensor, REF TS-E-D; Oximeter — Recall Details · AllClear