Magic3 Intermittent Catheters (2017-09-22)

MAGIC3 Intermittent Catheters Recall Summary MAGIC3 Intermittent Catheters have been recalled across Canada due to a device defect. This is a Class I recall, meaning the product could cause serious harm or death. The affected catheters were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-10-06

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a0a60e0f-ab28-4c13-906b-2a519f2a58a6