Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:17693
Brand Name:Biomet 3i Dental Implants
Model:Catalogue Numbers: BOST3211
Affected:Lots: 2014051395, 2014051817
Software version:
Recalling Organisation:ZimVie Australia Pty Ltd (NZ)
16 Huapai Street
Onehunga
Auckland 1061
Contact Information:0508 122 221
Manufacturer:Implant Innovations Inc
Issue:BIOMET 3i has identified a visually observable condition which may be present on a limited number of the above identified implants. The condition is caused by the implant coming into contact with residual machining fluid which was not adequately degreased from a portion of 1 lot of packaging cylinders. The lot of packaging cylinders was used in the packaging of the 4 implant lots.
The condition does not meet the cleanliness specification of BIOMET 3i. The residual machining fluid causes the implants to be discolored. Although the residual machining fluid is not a health hazard, the discolored implant is visually unacceptable to customers and, thus, BIOMET 3i is removing these suspect implants from the market.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:21/11/2014
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