Vitros Xt 7600 Integrated System (2019-03-20)

Recall Summary The VITROS XT 7600 Integrated System, a medical laboratory device, has been recalled across Canada due to a defect classified as a Class I safety issue. This device is used in hospitals and diagnostic laboratories to analyze patient samples. The recall affects all units of this system that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-04-05

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6463309b-849c-4aa8-8c2d-967aad36a356