Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13823 |
| Brand Name: | CareFusion Alaris GP Infusion System |
| Model: | Models: 80063UN01, 80263UN01, 80263UN01-G, 9002MED01, 9002MED01-G |
| Affected: | All pumps |
| Software version: | |
| Recalling Organisation: | CareFusion New Zealand 313 Limited Unit 4 / 110 Mays Road Onehunga AUCKLAND 1061 |
| Contact Information: | 0508 422 734 |
| Manufacturer: | CareFusion Switzerland 317 Sarl |
| Issue: | The manufacturer has determined that the Alaris GP Infusion System produces very small air bubles (less than 50ul) which are too small to trigger the lowest configurable air-in-line detection alarm being 50-500ul as configured by the user, or 1ml over 15 minutes. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/11/2012 |
