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

Recall Z-0820-2014 — Composix L/P with Echo PS 6" X 8" Product Code 0144680 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction of soft tissue defici

U.S. FDA — Device Enforcement · United States · 2014-01-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0820-2014
Date of alert: 2014-01-03
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: Product labeling does not match product configuration.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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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