Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:26441
Brand Name:DTR - Tibbs Cannula
Model:
Affected:Lot Numbers: 530227, 530537, 530657, 531229, 531790, 531568 and 532067
Software version:
Recalling Organisation:Downs Distributors Ltd
9 Airborne Road
North Harbour
AUCKLAND
Contact Information:0800 800 234
Manufacturer:DTR Medical Ltd
Issue:The manufacturer has identified an issue where the cone end of the Tibbs device separates from the luer connecter needle. The risk to the patient if separation occurs in use is the potential for the cone to get lodged in the Artery/Vein or travel to another part of the body, where further surgical intervention could be required to remove it.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:19/8/2020
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