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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Recalling Firm
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Z-2026-2023 - TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) REF TS-AP-10, 10 pcs; b) REF TS-AP-25, 25 pcs 1 07/07/2023 GE Healthcare Finland Oy
Z-2027-2023 - TruSignal AllFit Sensor: a) REF TS-AF-10, 10 pcs; B) REF AF-25, 25 pcs; Oximeter 1 07/07/2023 GE Healthcare Finland Oy
Z-2028-2023 - TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter 1 07/07/2023 GE Healthcare Finland Oy
Z-2029-2023 - TruSignal Wrap Sensor, REF TS-W-D; Oximeter 1 07/07/2023 GE Healthcare Finland Oy
Z-2034-2023 - TruSignal Integrated Ear Sensor with Ohmeda Connector REF TS-E4-H; Oximeter 1 07/07/2023 GE Healthcare Finland Oy
Z-2031-2023 - TruSignal Integrated Ear Sensor with GE Connector REF TS-E2-GE; Oximeter, Ear 1 07/07/2023 GE Healthcare Finland Oy
Z-2032-2023 - TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-GE; Monitor, physiological, patient(with arrhythmia detection or alarms) 1 07/07/2023 GE Healthcare Finland Oy
Z-2033-2023 - TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter 1 07/07/2023 GE Healthcare Finland Oy
Z-2030-2023 - TruSignal Ear Sensor, REF TS-E-D; Oximeter 1 07/07/2023 GE Healthcare Finland Oy
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