Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:22941
Brand Name:Catheter, intravascular, general-purpose
Model:
Affected:products containing the 3/8" vent plug 70000.8256
Software version:
Recalling Organisation:Getinge Australia Pty Ltd (NZ)
Unit D, Ground Floor, Building A, Millenium Centre
600 Great South Rd
Ellerslie
Auckland 1051
Contact Information:09 272 9039
Manufacturer:Maquet Cardio Pulmonary GmbH
Issue:The vent plug of the Arterial Cannula consists of sintered polyethylene, therefore the structure of the vent plug is porous and gas-permeable. After the de-airing process is completed the customer has to separate the vent plug from the cannula to connect the extracorporeal circuit.
In some cases it has come to the manufacturers attention that the vent plug has broken during the separation from the Arterial Cannula.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:7/5/2018
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