Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:22144
Brand Name:A&E Aorta Punch
Model:
Affected:lot numbers from 0090P through 0230P
Software version:
Recalling Organisation:Obex Medical Ltd
Level 3, 109 Carlton Gore Road
Newmarket
Auckland 1023
Contact Information:0800 656 539
Manufacturer:A & E Medical Corporation
Issue:There is potential packaging damage to have occurred during transportation, resulting in a loss of sterility. Recent testing has identified certain shipping configurations which may cause damage to the sterile barrier pouch if the Surgical Punches experience excessive movement from multiple drops during transport.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:24/10/2017
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