Unicel Dxi 600 And 800 Access Immunoassay Systems (2018-12-03)

Recall Summary Beckman Coulter is recalling UniCel DxI 600 and 800 Access Immunoassay Systems across Canada due to a potential defect in these medical laboratory devices. These systems are used in healthcare facilities to perform immunoassay testing on patient samples. Healthcare providers and laboratories using these devices are affected by this recall.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-01-08
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/60d46e0d-befd-4a39-bae5-69f913e054db