Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:13756
Brand Name:Kerr Bioplant Curved Syringe
Model:Part Numbers 216110 (0.125g), 216112, (0.25g), 216114 (0.50g), 216132 (2x0.25g)
Affected:All lots with expiration dates up to and including Oct-2017
Software version:
Recalling Organisation:Henry Schein Regional Ltd
243-249 Bush Road
Rosedale
North Shore City
Auckland 0632
Contact Information:0800 808 855
Manufacturer:Kerr Corporation
Brand Name:Kerr Bioplant Intro Pack
Model:Part number 216112B
Affected:All lots with expiration date up to and including Oct-2017
Software version:
Recalling Organisation:Henry Schein Regional Ltd
243-249 Bush Road
Rosedale
North Shore City
Auckland 0632
Contact Information:0800 808 855
Manufacturer:Kerr Corporation
Issue:The manufacturer is updating the instructions for use to include a statement that BioPlant material should not be disturbed for a period of 6-9 months after insertion to allow the material to ossify.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Healthcare Professional
Date Commenced:11/12/2012
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /