Fresenius Blood Pump Rotor

Fresenius Blood Pump Rotor Recall Fresenius is recalling blood pump rotors across Canada due to performance issues. The rotors are components used in blood pumping devices. This is classified as a Class I recall, the most serious category.

Product

Fresenius Blood Pump Rotor

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2024-05-06

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/06194d54-f12d-45aa-9b36-eece6f4caccf