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

Recall Z-1688-2014 — Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: 5955124 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

U.S. FDA — Device Enforcement · United States · 2014-04-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1688-2014
Date of alert
2014-04-24
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: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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