Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:28241
Brand Name:pRESET & pRESET LT
Model:
Affected:Stock code - PHE-PRES-5-40, PHE-PRE-LUX-4-20, PHE-PRE-LT-4-20, PHE-PRE-LT-3-20, PHE-PRE-6-30, PHE-PRE-4-20
Software version:
Recalling Organisation:Obex Medical Ltd
Level 3, 109 Carlton Gore Road
Newmarket
Auckland 1023
Contact Information:0800 656 539
Manufacturer:Phenox GmbH
Issue:The manufacturer has implemented a design change for the pRESET Thrombectomy Device whereby the introducer wire length has been changed from 1.8 to 2.0m
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:25/8/2021
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /