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Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number: 5955790 Indicated for use in the reconstruction of
Recalled June 11, 2014 · FDA recall Z-1694-2014 · Davol, Inc., Subs. C. R. Bard
Hazard
Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal. · FDA Class II
Sold at
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
Description
Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
Product
Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number: 5955790 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.
Manufacturer(s)
Davol, Inc., Subs. C. R. Bard, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →