Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:15021
Brand Name:Baxter Clearlink Solution Sets
Model:FNC3110
Affected:SR13A04021, SR13A02041, SR13A07032, SR13B14077
Software version:
Recalling Organisation:Baxter Healthcare Ltd
33 Vestey Drive
Mt Wellington
AUCKLAND
Contact Information:0800 229 837
Manufacturer:Baxter Healthcare Corporation
Issue:Manufacturer received feedback from a customer that an IV tube could not be loaded into a infusion pump because the side clamp was not correctly assembled. Manufacturer confirmed that the complaint sample and confirmed side clamp assembled in the reverse direction. The incorrect assembly would lead to incorrect direction of infusion such that blood may withdrawn froma patient and result in acute blood loss and/ or delay in treatment of life sustaining medication as worst case scenario.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Wholesale
Date Commenced:29/7/2013
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