Panoscreen I And II , 2-4% Suspension
Brand(s)
Last updated
Summary
Product
Panoscreen I And II , 2-4% Suspension
Issue
Medical devices - Performance issue
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
Get notified
Receive notifications for new and updated recalls and alerts by category.