Cell-dyn Emerald System - Instrument (2019-02-26)

CELL-DYN Emerald System Recall Summary Abbott Diagnostics is recalling the CELL-DYN Emerald System (a blood analysis instrument) across Canada due to a medical device issue. This recall affects healthcare facilities and laboratories that use this equipment. The FDA classified this as a Class I recall, indicating a serious safety concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-03-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/56ba5230-7363-4f6e-bd55-a4b9c3961322