Precisetype Hea Molecular Beadchip Test And Rhd Molecular Beadchip Test (2018-10-30)

Recall Summary PreciseType HEA Molecular BeadChip Test and RHD Molecular BeadChip Test kits are being recalled across Canada due to a defect in the medical devices. These tests are used to identify blood types and compatibility for transfusions. The recall affects all units of these products that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-11-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/72fdd76f-e7dd-41eb-9a42-5f44cb8c7eca