Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19010 |
| Brand Name: | CareFusion Alaris Syringe Infusion pump |
| Model: | 8110 |
| Affected: | Manufactured between Mar-2014 and Sep-2014 |
| 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: | CareFusion has identified an issue with the Alaris Syringe Pump module 8110 because the channel error will cause an audible and visual alarm on the Alaris PC unit and a channel error on the Alaris Syringe. Once cleared on the PCU the Syringe module remains unresponsive to key presses. This error could occur during an infusion causing an interruption of infusion. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 20/11/2015 |
