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

Recall Z-2674-2014 — DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level / 57 mm part 04.613.257 lot 3693878 TI Vectra" Plate 4 Level / 64 mm part 04.613.364 lot 8143905

U.S. FDA — Device Enforcement · United States · 2014-09-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2674-2014
Date of alert
2014-09-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Synthes, Inc.
Product category
device
Product type
Devices
Reported risk: DePuy Synthes is initiating a voluntary medical device recall of certain lots of the TI Vectra Plates, which is a part of the DePuy Synthes Vectra Anterior Cervical Plate Family of Systems. The Vectra Systems are intended for anterior screw fixation to the cervical spine (C2-C7). It was discovered in certain lots, that the clips are potentially missing from the TI Vectra Plates resulting in the i
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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