Guider Softtip Xf
Guider SoftTip XF Recall Summary Guider SoftTip XF catheters are being recalled across Canada due to a defect that may cause the catheter tip to separate or detach during use. This recall affects all users of this product in Canada. The manufacturer has classified this as a Class I recall, which indicates a serious safety concern.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-11-09
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/bf9b315a-fa5f-469d-a6f7-973f26f33ff3