Health product recall

Panoscreen I And II , 2-4% Suspension

Brand(s)
Last updated

Summary

Product
Panoscreen I And II , 2-4% Suspension
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

Panoscreen I And II , 2-4% Suspension

18915

0002380

Issue

Immucor Inc. has indicated that this medical device recall is to communicate that some vials of this lot (18915) exhibit an unexpected dark color (hemolysis) and darkening of the red blood cells. It has been confirmed that there is fungal growth in the vials demonstrating dark color. This issue is random across kits in this lot and is not present in all vials within the kit. Fungal contamination may lead to erroneous results.

Recall start date: June 12, 2024

 

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Haematology
Companies
Immucor Inc.
3130 Gateway Drive, Norcross, Georgia, United States, 30071
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75802

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