Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18724
Brand Name:Stryker SBi u head stem and sigmoid notch radial stem
Model:UHAS3; 3900305
Affected:19820S2; 18362, 22834401
Software version:
Recalling Organisation:Stryker New Zealand Ltd
515 Mount Wellington Highway
Mount Wellington
AUCKLAND 1060
Contact Information:0800 787 9287
Manufacturer:Small Bone Innovations Inc
Issue:Stryker became aware during laboratory testing that there is a potential that the packaging integrity (sterile barrier) of the packaging type KIT I may be compromised by transportation. A compromised sterile barrier could result in the surgeon selecting a back-up device or, if not recognized, an unintended implantation of a potentially non sterile device. The packaging type KIT I consists of a white cardboard box, an outer peel pouch, and an inner peel pouch.
Recall action type:Alert
Recall action:Manufacturer to issue advice regarding use
Level of recall:Healthcare Professional
Date Commenced:24/6/2015
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