FDA Recall
Terminated
Hemashield Platinum Woven Double Velour TAAA Vascular Grafts.
Recall: Z-2065-2010
·
Initiated May 24, 2010
Recall
- Recall Number
- Z-2065-2010
- Event Number
- 56004
- Firm
- Maquet Cardiovascular, LLC
- FEI Number
- 2242352
- Product Code
- MAL
- Status
- Terminated
- Root Cause
- Package design/selection
- Initiated
- May 24, 2010
- Posted
- July 22, 2010
- Terminated
- July 14, 2011
- Address
- 45 Barbour Pond Dr, Wayne, NJ, 07470-2094
Description
Hemashield Platinum Woven Double Velour TAAA Vascular Grafts.
Reason
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.
Action
Letters 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.
Distribution
Nationwide Distribution.
Quantity
xx