Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:14890
Brand Name:Zimmer NexGen Cruciate Retaining CR Micro Femur
Model:64 models
Affected:All lots
Software version:
Recalling Organisation:Zimmer Biomet New Zealand Company
210 Khyber Pass Road
Grafton
Auckland
Contact Information:09 925 5200
Manufacturer:Zimmer Inc
Brand Name:Zimmer NexGen Cruciate Retaining CR Micro Articular Surface
Model:99 models
Affected:All lots
Software version:
Recalling Organisation:Zimmer Biomet New Zealand Company
210 Khyber Pass Road
Grafton
Auckland
Contact Information:09 925 5200
Manufacturer:Zimmer Inc
Brand Name:Zimmer NexGen Micro Patella
Model:8 models
Affected:All lots
Software version:
Recalling Organisation:Zimmer Biomet New Zealand Company
210 Khyber Pass Road
Grafton
Auckland
Contact Information:09 925 5200
Manufacturer:Zimmer Inc
Brand Name:Zimmer NexGen Implant trial devices
Model:58 models
Affected:All lots
Software version:
Recalling Organisation:Zimmer Biomet New Zealand Company
210 Khyber Pass Road
Grafton
Auckland
Contact Information:09 925 5200
Manufacturer:Zimmer Inc
Issue:Zimmer is recalling micro femurs, micro patellae and micro articular surfaces to prevent use of these components in combinations that are not approved by the manufacturer. Devices will be available for revision surgeries only.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:24/6/2013
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