Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:24924
Brand Name:Infusion pump administration set_IIa
Model:AS LVP 20D 3SS CV, AS LVP 20D LOW SORB, AS LVP 20D CV, AS LVP 20D DEHP 2VS, AS LVP 20D DEHP 2INJ, AS LVP 20D DEHP SS, AS LVP 20D 2SS CV, AS LVP 20D DEHP 2SS CV
Affected:
Software version:
Recalling Organisation:Becton Dickinson Ltd
Unit 4 / 110 Mays Road
Onehunga
Auckland 1061
Contact Information:0800 572 468
Manufacturer:BD Switzerland Sarl
Issue:The manufacturer has identified an issue is caused by a variation in the wall thickness of the BD Alaris Pump Model 8100 Infusion Sets silicone pumping segment. There is potential for an incomplete occlusion leading to unintended delivery of medication when the pump is not running placed on pause with roller clamp opened or faster than expected drug delivery flow when the pump is infusing.
Recall action type:Recall
Recall action:Product to be destroyed
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:2/8/2019
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