Neuro-fiberscope (2019-08-23)

Neuro-Fiberscope Recall Summary A medical device called the Neuro-Fiberscope has been recalled across Canada due to a safety issue. This is a Class I recall, which is the most serious type. The device was distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-09-12

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d9a45cc0-fdbc-4c58-aea1-d33535a97e0a