Ellex Integra Pro Lp5532 (2016-03-16)

Recall Summary ELLEX INTEGRA PRO LP5532 medical devices are being recalled across Canada due to a safety concern that poses a risk to patients. This is a Class I recall, which is the most serious type. The recall affects all units of this device that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-04-04

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/dec3cba1-d5ee-43ce-b28d-017ea72b6fde