Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:24450
Brand Name:Biomet Trauma - Surgical Instrument handle
Model:T7 Cannulated Driver AO and T7 Driver Solid AO
Affected:All Lots - HCS BAROUK 2, All Lots - HCS BAROUK 2, All Lots - HCS BAROUK 2 2.5mm only
Software version:
Recalling Organisation:Zimmer Biomet New Zealand Company
210 Khyber Pass Road
Grafton
Auckland
Contact Information:09 925 5200
Manufacturer:Biomet Trauma
Issue:The manufacturer has identified a potential fracture, bending or shearing of the T7 Driver. The T7 Driver is being redesigned. All distributed product remaining in the field is being removed
Recall action type:Recall
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:12/4/2019
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