Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20941 |
| Brand Name: | Alaris Infusion Pumps |
| Model: | |
| Affected: | Models 8000 and 8015 |
| Software version: | |
| Recalling Organisation: | CareFusion New Zealand 313 Limited Unit 4 / 110 Mays Road Onehunga AUCKLAND 1061 |
| Contact Information: | 0508 422 734 |
| Manufacturer: | CareFusion 303 Inc |
| Issue: | The manufacturer has received reports of the Alaris System PC units operating on battery power where the low battery alarm and / or the very low battery alarm are not being triggered before the battery is discharged and all infusion channels are stopped. This issue does not occur if the device is plugged into an AC outlet. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 19/12/2016 |
