Peg Extender/peg Guide Extender (2019-11-26)

Recall Summary A peg extender/peg guide extender medical device is being recalled across Canada. The recall was classified as Class I, meaning there is a serious potential health risk associated with the device. The specific reason for the recall relates to issues with the medical device itself, though the exact details of the hazard are not provided in this notice.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-01-06
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6d2713e9-e9be-49e4-8667-0636e0c7184d