Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18148
Brand Name:BD Q-Syte Luer Access Split Septum Device
Model:Reference: 385100
Affected:Lot: 4128925
Software version:
Recalling Organisation:Becton Dickinson Ltd
Unit 4 / 110 Mays Road
Onehunga
Auckland 1061
Contact Information:0800 572 468
Manufacturer:Becton Dickinson Infusion Therapy Systems Inc
Issue:The manufacturer advises that some units of BD Q-Syte Luer Access Split Septum Device have an off-centered slit in the silicon septum resulting in a thinner column wall. When actuated, units with a thinner column wall may tear leading to leakage of insuate/medication or blood from the side vent opening.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:25/2/2015
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