Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:22766
Brand Name:Stryker Medical - Performance Load
Model:
Affected:All serial numbers beginning with 16 are within scope of this action e.g. 160139706
Software version:
Recalling Organisation:Stryker New Zealand Ltd
515 Mount Wellington Highway
Mount Wellington
AUCKLAND 1060
Contact Information:0800 787 9287
Manufacturer:Stryker Medical
Issue:After installation of the Power-LOAD, the Floor Plate Attachment Brackets (PN: 6390-101-108) which allow the Power-LOAD anchor to be secured to the Power-LOAD floor plate may be found to be broken after removing the anchor. All Power-LOAD units manufactured from January 1, 2016 to December 31, 2016, may potentially exhibit this issue.
The manufacturer has expanded the scope of this Recall for Product Correction. Units manufactured between January 1, 2017 and August 16, 2017 have been added to this PFA.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:17/12/2018
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