Hla Fusion Software (version 2.0.0 Sp4.1) (2013-07-29)

HLA Fusion Software Recall Summary HLA Fusion Software version 2.0.0 SP4.1 has been recalled across Canada due to a safety issue with this medical device software. The recall is classified as Class I, meaning there is a serious potential for harm. This recall affects all Canadian users of this specific software version.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2013-09-19

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d8e1b630-0e6a-4d50-9f05-7b32fb13c90a