Sysmex Di-60™ Main Unit

Sysmex DI-60™ Main Unit Recall The Sysmex DI-60™ Main Unit, a medical device distributed across Canada, has been recalled due to a performance issue. This Class I recall affects all units of this device that were distributed in Canada. The specific performance concern has prompted Health Canada to classify this as a serious safety issue requiring immediate action.

Product

Sysmex DI-60™ Main Unit

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2025-10-24

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d1e9df61-2d9e-4dee-a001-e7c9aab668f3