AlboGraft Woven with Collagen — Class I medical device recall Z-1768-2013
Terminated recall by LeMaitre Vascular, Inc., reported 2013-07-31, distributed in GA. Blood blushing/leaking from the surface of the graft after implantation
| Recall number | Z-1768-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LeMaitre Vascular, Inc., Burlington, MA, United States |
| Recall initiated | 2013-06-17 |
| Classified | 2013-07-22 |
| Reported by FDA | 2013-07-31 |
| Terminated | 2016-08-15 |
| Distributed | GA |
| Countries outside the US | BG, BR, DE, ES, FR, GR, IT, LB, PL, TR |
| Quantity | 1 units |
| Reason classes | packaging |
| Lot numbers | 2015-04, 56890A |
| Model numbers | ATC3018 |
Product
AlboGraft Woven with Collagen, Straight 30x18 Catalog Number: ATC3018 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
Reason for recall
Blood blushing/leaking from the surface of the graft after implantation
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1768-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.