Health product recall

Liquiband Fix8 Open Hernia Mesh Fixation Device

Last updated

Summary

Product
Liquiband Fix8 Open Hernia Mesh Fixation Device
Issue
Medical devices - Manufacturing defect
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected Products

Lot or Serial Number

Model or catalog number

Liquiband Fix8 Open Hernia Mesh Fixation Device

P00221600, P00225605, P00221983, P00221396, P00221182, P00225801, P00221756, P00226740, P00221313

FX002

Issue

During verification testing, a non-conformance was detected. Failure mode was uncontrolled leakage of glue from the distal tip of the Fix8 open (FX002) device.

Recall start date: Feb 3, 2022

Additional information

Details
Original published date: 2022-02-16
Alert / recall type
Health product recall
Category
Health product - Medical device - General and plastic surgery
Companies

Advanced Medical Solutions Limited

Western Wood Way, Plymouth, Devon

Great Britain, PL7 5BG

Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type I
Identification number
RA-63929