Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18716
Brand Name:Biomet Medium Bone Plate forceps
Model:816301006
Affected:099216, 093776, 093717, 093716, 088526, 081179, 072525, 072524
Software version:
Recalling Organisation:Biomet New Zealand Ltd
Contact Information:0275 522 595
Manufacturer:Biomet Trauma
Issue:Biomet is recalling specific lots of Medium Bone Plate Forceps which have been assembled with the incorrect grip arm component.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Sponsor Control
Date Commenced:19/6/2015
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