Biotestcell P3

Biotestcell P3 medical devices are being recalled in Canada due to safety concerns. The recall applies to all units distributed across Canada. This is a Class I recall, which is the most serious classification for medical devices.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2012-10-01

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4a2565ea-a09a-450b-9f60-a93ec68be6d6