Health product recall

LiquiBandFIX8® Open Hernia Mesh Fixation Device

Last updated

Summary

Product
LiquiBandFIX8® Open Hernia Mesh Fixation Device
Issue
Medical devices - Premature failure
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected Products

Lot or Serial Number

Model or catalog number

LiquiBandFIX8® Open Hernia Mesh Fixation Device

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

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:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies

Advanced Medical Solutions Ltd.

Plymouth, Devon

United Kingdom, PL7 5BG

Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type III
Identification number
RA-63914

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