Data Foundry

Medical device recalls 2014

DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm… — Class II medical device recall Z-2674-2014

Terminated recall by Synthes, Inc., reported 2014-10-01, distributed in AL, CA, CO, IL, KS, LA, MA, NC…. DePuy Synthes is initiating a voluntary medical device recall of certain lots of the TI Vectra Plates, which i

Recall numberZ-2674-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSynthes, Inc., West Chester, PA, United States
Recall initiated2014-09-02
Classified2014-09-22
Reported by FDA2014-10-01
Terminated2015-09-02
DistributedAL, CA, CO, IL, KS, LA, MA, NC, NE, OR, SC, TX, VA
Countries outside the USCA
Quantity16
Lot numbers3693878TI, 8143905
Model numbers04.613.184, 04.613.257, 04.613.364, 3337672TI

Product

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

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2674-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.