Perseus A500 (2020-07-09)

Perseus A500 Recall Summary The Perseus A500 medical device has been recalled across Canada due to safety concerns. This Class I recall affects all units of this device that were distributed nationwide. Further details about the specific safety issue and affected user populations are not provided in the available information.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-08-14

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0ac99d45-85cb-4287-883c-e7004d6111da