Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2412-2012 — 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 reconstructio

U.S. FDA — Device Enforcement · United States · 2012-09-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2412-2012
Date of alert: 2012-09-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Davol, Inc., Subs. C. R. Bard, Inc.
Product category: device
Product type: Devices

Reported risk: 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 product

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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