Ureteroreno Fiberscope
UreteroReno Fiberscope Recall Summary The UreteroReno Fiberscope, a medical device used in urological procedures, is being recalled across Canada due to a Class I safety issue. The recall affects medical facilities and healthcare providers that use this instrument. [Note: The specific reason for the recall is not provided in the information given; typically Class I recalls indicate a serious risk of injury or death.]
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-01-12
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9c4ffc70-2248-4e99-aa0f-0fc7ebcfcb2b