Id-diapianel (p) (2016-07-04)

Recall Summary ID-DIAPIANEL (P) is being recalled across Canada due to issues with the medical device. This is a Class I recall, which is the most serious classification. The product was distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-07-19

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e16d5c2d-f9b6-4618-8b13-2ccef13b0da6