Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:26641
Brand Name:Alaris System Infusion Pumps_CFN San Diego
Model:System PC Unit Model 8015, manufactured from April, Alaris Syringe Module Model 8110 manufactured from March 1, 2010, to present, Alaris PCA Module Model 8120 manufactured from March 1, 2010, to present,BD Alaris System PC Unit Model 8015,
Affected:
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:There are 3 key issues being outlined in this Product Correction. As the manufacturing date of each issue vary some customer may be impacted by one, two or all issues. To streamline customer communication, customer will be provided with letter specific to the issue impact.
Issue 1 – PCU keypad
Issue 2 – LVP keypad
Issue 3: Syringe / PCA Sizer sensor
Recall action type:Correction
Recall action:Product to be exchanged
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:29/9/2020
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