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

Recall Z-1470-2020 — NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.

U.S. FDA — Device Enforcement · United States · 2020-02-07 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1470-2020
Date of alert
2020-02-07
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Integra LifeSciences Corp.
Product category
device
Product type
Devices
Reported risk: Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.
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.

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