Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:16051
Brand Name:Stryker Torque Wrench
Model:Xia 03807028, Xia 3 48237028, Mantis Redux 48287028
Affected:092793, 098525, 11A957, 11E035, 11E039, 11E042, 11E045, 11E046, 11E047 , 123746, 127051 and R11E036
Software version:
Recalling Organisation:Stryker New Zealand Ltd
515 Mount Wellington Highway
Mount Wellington
AUCKLAND 1060
Contact Information:0800 787 9287
Manufacturer:Stryker Spine SAS
Issue:Manufacturer previously initiated a lot specific recall (Ref #15444) after reports received that the hex tip of the torque wrench of an identified lot number subset had been fracturing during final tightening.The establised cause for the fracture was due to grain boundary attack as a result of the heat treat process. Since that time additional testing has continued and the manufacturer has made the decision to distribute a recall letter to all customers that have a procedure pack in their possession that may contain the affected product and inform them of the recall expansion. Additionally the manufacturer has confirmed that the supplier will use a new heat treatment vendor for which there is a validated heat treatment process.
31/07/2015 - Identified that LOT 11E035 was not previous included in the recall letters associated with this recall. Recall letter updated to include all affected lots and attached a list of all current locations
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:22/1/2014
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