Various Medlines' Custom Procedure Packs (2018-04-06)

Medline Custom Procedure Packs Recall Medline is recalling various custom procedure packs across Canada because they are classified as medical devices that do not meet regulatory requirements. The recall affects custom procedure packs distributed throughout Canada. This is a Class I recall, which is the most serious classification.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-05-04

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f658f945-9f5c-4b26-a5f4-0d71718d27ba