Official recall record
Biodesign® Hiatal Hernia Graft
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-12-19
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
There is a discrepancy between the correct product shelf life versus the shelf life presented on the finished product labeling. The affected products expire prior to the expiration date printed on the product labeling. This creates the potential for devices to be used beyond their intended expiration date. Recall start date: December 10, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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