Davol, Inc., Subs. C. R. Bard, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1692-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product 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.

Product Classification:

Class II

Date Initiated: April 24, 2014

Date Posted: June 11, 2014

Recall Number: Z-1692-2014

Event ID: 68124

Reason for Recall:

Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.

Status: Terminated

Product Quantity:

Code Information:

Lot Number: HUXK0744, HUXL1004

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated