FDA Enforcement
Class II
Terminated
Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number: 5955610 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Recall: Z-1692-2014
·
Reported June 11, 2014
Enforcement
- Recall Number
- Z-1692-2014
- Event ID
- 68124
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Davol, Inc., Subs. C. R. Bard, Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- June 11, 2014
- Initiation Date
- April 24, 2014
- Classification Date
- June 2, 2014
- Termination Date
- December 23, 2015
- Address
- 100 Crossings Blvd, Warwick, RI, 02886-2850, United States
Description
Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number: 5955610 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Reason
Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
Code Info
Lot Number: HUXK0744, HUXL1004
Distribution
Worldwide Distribution - USA (nationwide) and Internationally to AUSTRIA, BELGIUM, CANADA, CYPRUS, ESTONIA, FINLAND, FRANCE, GERMANY, GREECE, IRELAND, ITALY, LUXEMBOURG, NETHERLANDS, NORWAY, POLAND, PORTUGAL, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, and UNITED KINGDOM