Gelita Tuft-It®
Brand(s)
Last updated
Summary
Product
Gelita Tuft-It®
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Gelita Tuft-It® |
F00080/1 |
GF-7365 |
Issue
The endotoxin limit/specification appears to have been exceeded in re-testing using a new method.
Recall start date: September 9, 2022
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies
Gelita Medical GmbH
Uferstrasse 7, Eberbach, Germany, 69412
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-64567
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