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GE Healthcare Finland Oy recalls TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) REF TS-AP-10, 10 pcs; b) REF TS-AP-25, 25 pcs
Recalled July 12, 2023 · FDA recall Z-2026-2023 · GE Healthcare Finland Oy
Hazard
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. · FDA Class I
Units
23537 devices
Sold at
Worldwide
Description
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
Product
TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) REF TS-AP-10, 10 pcs; b) REF TS-AP-25, 25 pcs
Manufacturer(s)
GE Healthcare Finland Oy
Made in
Finland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →