Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:27644
Brand Name:Alaris System Infusion Pumps_CFN San Diego
Model:
Affected:Product Codes- 8100BDAIXEN121, 8100BDADXEN933
Software version:
Recalling Organisation:Becton Dickinson Ltd
Unit 4 / 110 Mays Road
Onehunga
Auckland 1061
Contact Information:0800 572 468
Manufacturer:CareFusion 303 Inc
Issue:The affected BD Alaris™ Pump Module keypads may exhibit keypad lifting, which could result in one or more keys becoming unresponsive or stuck (i.e., constantly pressed state) due to fluid ingress.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:22/4/2021
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