Health product recall

iQ200 Series Analyzers and DxU 840m/850m Iris Analyzers

Last updated

Summary

Product
iQ200 Series Analyzers and DxU 840m/850m Iris Analyzers
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

DxU 840m Iris

More than 10 numbers, contact manufacturer.

C76947

iQ200 SPRINT 2008 Tested

More than 10 numbers, contact manufacturer.

700-3325

iQ200 SELECT 2008 Tested

More than 10 numbers, contact manufacturer.

700-3345

DxU 850m Iris

More than 10 numbers, contact manufacturer.

C49513

iQ200 ELITE 2008 Tested

More than 10 numbers, contact manufacturer.

700-3375

Issue

Beckman Coulter received customer complaints of lamina fluid leaks in iQ200 Series and DxU 840m/850m Analyzers. The investigation found that a structurally compromised rinse-line check valve may allow fluid to migrate internally and leak onto the table or floor, potentially resulting into exposure to physical or mechanical or chemical hazards.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Chemistry
Companies

Beckman Coulter Ireland, Inc.

Lismeehan, Co. Clare, Ireland,

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82520

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