Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K093881 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 |
TruSignal Ear Sensor, REF TS-E-D; Oximeter | 1 | 07/07/2023 | GE Healthcare Finland Oy |
TruSignal Wrap Sensor, REF TS-W-D; Oximeter | 1 | 07/07/2023 | GE Healthcare Finland Oy |
TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter | 1 | 07/07/2023 | GE Healthcare Finland Oy |
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