Cobas P 612 Pre-analytical System Lcp1 (2018-07-12)

Recall Summary The Cobas p 612 pre-analytical system LCP1 has been recalled across Canada due to a medical device issue. This system is used in laboratory settings to prepare samples for testing. The recall is classified as Class I, meaning there is a serious potential for harm.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-07-27

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/391e2d9b-4523-4436-b36b-3e53cdee45b0