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Liquiband fix8 open hernia mesh fixation device
Official notice
14 Feb 2022
Last checked
14 Feb 2022
An official Health Canada notice concerns Liquiband fix8 open hernia mesh fixation device. 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 Published 2022-02-14.
What to do now
Contact the manufacturer if you require additional information.
Recall number
63929
Official notice
2022-02-14
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Advanced Medical, Liquiband Fix8 Open Hernia Mesh Fixation Device.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
View full official noticeRelated recalls
11 Feb 2022
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