Davol, Inc., Subs. C. R. Bard, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2413-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Bard Ventralight ST Mesh. - Ellipse 7" x 9" (17.8 cm x 22.9 cm) Product Code 5954790. The Bard Ventralight ST Mesh is a dual-component (absorbable and nonabsorbable) sterile prosthesis. The device classification name is "Mesh, Surgical, Polymeric." It is in tented for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.

Product Classification:

Class II

Date Initiated: September 4, 2012

Date Posted: September 26, 2012

Recall Number: Z-2413-2012

Event ID: 63069

Reason for Recall:

Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh product and the 7" x 9" package contains 8" x 10" VENTRALIGHT ST Mesh

Status: Terminated

Product Quantity: 49 units

Code Information:

Lot # HUWE1780

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated