Devices

Device Recall Advanta SuperSoft Grafts

Model / Serial
Product manufactured between April 3, 2012 and May 14, 2013 and can be identified by their expiration date; between April 2017 and May 2018.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution - USA (nationwide) and internationally to the following countries: American Samoa Antilles Argentina Australia Austria Bangladesh Belgium Bolivia Brazil Canada Chile Colombia Egypt El Salvador Finland France Germany Great Britain Greece Guatemala Hong Kong India Indonesia Ireland Italy Jamaica Japan Korea Lebanon Libya Malaysia Mauritius Mexico Neal New Zealand Nicaragua Norway Pakistan Panama Peru Philippines Poland Portugal Puerto Rico Romania Russia Saudi Arabia Singapore Slovenia South Africa Spain Switzerland Taiwan Thailand the Netherlands Trinidad Tunisia
Product Description
Advanta SuperSoft Grafts <6mm || Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.
Manufacturer
Atrium Medical Corporation
2 Events
- Recall of Device Recall Advanta SuperSoft Grafts
- Recall of Device Recall Advanta SuperSoft Grafts

Manufacturer

Atrium Medical Corporation

Manufacturer Address
Atrium Medical Corporation, 5 Wentworth Dr, Hudson NH 03051-4929
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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