Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:28777
Brand Name:Magec Rod
Model:
Affected:IFU update
Software version:
Recalling Organisation:NuVasive (Aust/NZ) Pty Ltd
Unit 1.2 Ground Floor
1 Kenwyn Street
Parnell
Auckland 1052
Contact Information:64 027 509 0033
Manufacturer:Nuvasive Specialized Orthopaedics Inc
Issue:The manufacturer has made changes to their instructions for use (IFU) documents. The IFU changes align the duration of implantation with the rest of the world.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:30/12/2021
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /