Tosoh Aia 360 Analyzer (2018-08-29)

Recall Summary Tosoh AIA 360 Analyzer devices are recalled due to a medical device issue. This recall applies to units distributed across Canada. The FDA classified this as a Class I recall, which is the most serious category.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-09-28

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/eaeb6ff3-73bf-45df-bfd3-b2786364e166