Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21026
Brand Name:Zimmer Hip Arthroplasty (femoral stems & heads)
Model:
Affected:updated surgical techniques with reference 06.01109.012X - Ed 2016.11 - rev. 04 for the Revitan Straight .
Software version:
Recalling Organisation:Zimmer Biomet New Zealand Company
210 Khyber Pass Road
Grafton
Auckland
Contact Information:09 925 5200
Manufacturer:Zimmer GmbH
Issue:The manufacturer is providing information on the use of the Revitan Revision System and is jointly provided with the latest updated surgical techniques with reference 06.01109.012X - Ed 2016.11 - rev. 04 for the Revitan Straight.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Healthcare Professional
Date Commenced:20/1/2017
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