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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:112452

Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. 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.

Official recall number

Z-2412-2012

Evidence summary

Product code
FTL
Recall status
Terminated
Event initiated
September 04, 2012
Root cause
Mixed-up of materials/components
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2412-2012