Syringe Pumps_bd Swissco

Recall Summary BD SwissCo Syringe Pumps with certain keypad components are being recalled because the keypads may malfunction, causing the pump to enter an unintended mode, become unresponsive, or display an error—potentially delaying or interrupting medication delivery. The recall affects specific model numbers (CCNEXUS1-S, PKNEXUS1, 8002TIG03-G, 8005TIG03, 8005PK201) distributed to hospitals, pharmacies, and laboratories in New Zealand. Interrupted infusions could cause serious harm, particularly for patients receiving time-sensitive medications like vasoactive drugs or anesthesia.

Recalling firm

Becton Dickinson Ltd

Product

Syringe Pumps_BD SwissCo. [Device]. Model: Catalog Number - CCNEXUS1-S, PKNEXUS1, 8002TIG03-G, 8005TIG03, 8005PK201

Reason

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...

Classification

Class I

Category

medical device recall

Country

New Zealand

Agency

MEDSAFE

Recall date

2026-02-17

Status

Ongoing

Distribution

New Zealand - Hospital/Pharmacy/Laboratory

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/0b85e5e6-d0a6-4d9b-b206-acf195dec262