TruSignal Wrap Sensor recall
TruSignal Wrap Sensor, REF TS-W-D; Oximeter
Why was TruSignal Wrap Sensor recalled?
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN 00840682103121
- Product
- TruSignal Wrap Sensor, REF TS-W-D; Oximeter
- Recalling firm
- GE Healthcare Finland Oy
- Quantity
- 5039 units
- Distribution
- Worldwide
- Recall date
- July 12, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)