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U.S. Department of Health and Human Services

Class 1 Device Recall LeMaitre Albograft

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 Class 1 Device Recall LeMaitre Albograftsee related information
Date Initiated by FirmJune 17, 2013
Date PostedJuly 22, 2013
Recall Status1 Terminated 3 on August 15, 2016
Recall NumberZ-1764-2013
Recall Event ID 65553
510(K)NumberK093231 K103080 
Product Classification Graft, vascular, synthetic/biologic composite - Product Code MAL
ProductAlboGraft Knitted with Collagen, Straight 60x08 Catalog Number: AMC6008 AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
Code Information Lot number/Expiration Date  56890A 2015-04
Recalling Firm/
Manufacturer		 LeMaitre Vascular, Inc.
63 2nd Ave
Burlington MA 01803-4413
For Additional Information ContactLaurie Churchill
781-425-1670 Ext. 108
Manufacturer Reason
for Recall		Blood blushing/leaking from the surface of the graft after implantation
FDA Determined
Cause 2		Process control
ActionLeMaitre Vascular, Inc.sent an Urgent Field Safety Notice daed June 19, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to identify and return the affected device to MeMaitre Vascular which they will replace with a new unit. Customers with questions were instructed to call 781-221-2266, ext. 183. For questions regarding this recall call 781-425-1670, ext 108.
Quantity in Commerce2 units
DistributionWorldwide distribution: USA including PA and countries of: BRAZIL, BULGARIA, FRANCE, GEORGIA, GERMANY, GREECE, ITALY, LEBANON, NETHERLAND, POLAND, SPAIN, and TURKEY.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = MAL
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