GE Healthcare TruSignal™ SpO₂ Sensors
Brand(s)
Last updated
Summary
Product
GE Healthcare TruSignal™ SpO₂ Sensors
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Sensitive Skin Disposable Sensor | Contact the manufacturer. | TS-SE-3 TS-W-D |
| AllFit Disposable Sensor | Contact the manufacturer. | TS-AF-10 TS-AF-25 |
| Integrated Ear Sensors | Contact the manufacturer. | TS-E-D TS-E4-GE TS-E2-GE TS-E4-N TS-E4-H |
| Adult/Ped Disposable Sensor | Contact the manufacturer. | TS-AP-10 TS-AP-25 |
Issue
Potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement related to TrusignalTM SpO2 sensors.
Recall start date: June 5, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Health products - Medical devices - General and plastic surgery
Companies
GE Healthcare Finland Oy
Kuortaneenkatu 2, Helsinki, Finland, 00510
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73860
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