Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16553 |
| Brand Name: | Baxter Colied Tube INFUSOR System cs |
| Model: | 2C1071KJP 1C1071KJ 1C1073KJP 2C1075KJP 2C1080KJP 2C1082KJP and 2C1082KJ |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Baxter Healthcare Ltd 33 Vestey Drive Mt Wellington AUCKLAND |
| Contact Information: | 0800 229 837 |
| Manufacturer: | Baxter Healthcare Corporation |
| Issue: | Manufacturer has received complaints for infusion flow rates greater than intended for the listed portable elastomeric infusion systems. Manufacturer is requesting that healtrhcare providers consider the Instructions for Use which explain facts that may impact resulting flow rate. Point #5 of the Instructions for Use is incorrect and manufactrer will be making a change to this to reflect this information. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/4/2014 |
