Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:36544
Brand Name:Syringe Pumps_BD SwissCo
Model:Catalog Number - CCNEXUS1-S, PKNEXUS1, 8002TIG03-G, 8005TIG03, 8005PK201
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:Specific lots of the keypad components may exhibit unintended behaviour impacting the “On/Off”, “Hold” and “Run” keys.
Specifically, the affected pumps may experience one or more of the following failure modes:
- The pump may enter “Tech Mode” autonomously during powerup.
- Keypad buttons may become unresponsive, preventing normal
operation.
- A “KY1” error may be displayed, indicating a stuck key.
A faulty keypad on the BD Alaris Syringe Pump may cause delays in starting or interruptions during infusion, with the severity of harm depending on the drug type, patient condition, and duration of the interruption. Potential outcomes range from no harm to critical injury, particularly when short half-life vasoactive drugs or TIVA are involved, as these are used in high-acuity patients and can lead to hemodynamic instability or reduced anaesthesia within minutes
Recall action type:Correction
Recall action:Product to be exchanged
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:17/2/2026
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