[Recalled] AlboGraft Knitted with Collagen, Bifurcate 18x10 Catalog Number: AMC1810 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries. — Blood blushing/leakin
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | AlboGraft Knitted with Collagen, Bifurcate 18x10 Catalog Number: AMC1810 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries. |
|---|---|
| Brand / manufacturer | LeMaitre Vascular, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1758-2013 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 17 June 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Blood blushing/leaking from the surface of the graft after implantation
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.