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U.S. Department of Health and Human Services

Class 2 Device Recall Hemashield Gold Woven and Knitted Double Vascular Grafts.

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 Class 2 Device Recall Hemashield Gold Woven and Knitted Double Vascular Grafts.see related information
Date Initiated by FirmMay 24, 2010
Date PostedJuly 22, 2010
Recall Status1 Terminated 3 on July 14, 2011
Recall NumberZ-2066-2010
Recall Event ID 56004
510(K)NumberK954848 
Product Classification Graft, vascular, synthetic/biologic composite - Product Code MAL
ProductHemashield Gold Woven and Knitted Double Vascular Grafts.
Code Information xx
Recalling Firm/
Manufacturer		 Maquet Cardiovascular, LLC
45 Barbour Pond Dr
Wayne NJ 07470-2094
For Additional Information ContactSusan Eichler Huston
973-709-7487
Manufacturer Reason
for Recall		Various Hemashield products may develop glycerol droplets on the inner blister of the package if not stored under proper conditions, which could lead to the prolongation of surgery and potentially compromise patient safety.
FDA Determined
Cause 2		Package design/selection
ActionLetters were sent by Federal Express commencing July 12, 2010. Distribution has to be obtained from Boston Scientific. Questions are directed to the local Sales/Service Representative, or to the firm's Customer Service at 1-888-880-2874.
Quantity in Commercexx
DistributionNationwide Distribution.
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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