Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:25618
Brand Name:Aortic Punch
Model:
Affected:Multiple Lot Numbers
Software version:
Recalling Organisation:Teleflex Medical New Zealand
OFFICE 011, 110 CARLTON GORE ROAD
Newmarket
Auckland 1023
Contact Information:027 476 4009
Manufacturer:Teleflex Medical
Issue:The manufacturer has become aware of instances where the sterility of the Premium Diamond Edge Aortic Punch may be compromised.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:30/1/2020
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