Health product recall

Gelita Tuft-It®

Last updated

Summary

Product
Gelita Tuft-It®
Issue
Medical devices - Performance issue
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
F00077/1
F00079/1
F00116/2

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: 2022-09-23
Alert / recall type
Health product recall
Category
Health product - Medical device - 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