FDAFDA · Food and drugs·Recall number Z-1768-2013
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.
Published July 31, 2013 · Recall initiated: June 17, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Blood blushing/leaking from the surface of the graft after implantation
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- LeMaitre Vascular, Inc.
- Distributor
- Worldwide distribution: USA including PA and countries of: BRAZIL, BULGARIA, FRANCE, GEORGIA, GERMANY, GREECE, ITALY, LEBANON, NETHERLAND, POLAND, SPAIN, and TURKEY.
- Lot
- Lot number/Expiration Date 56890A 2015-04
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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