Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21194 |
| Brand Name: | Alaris Infusion Pumps |
| Model: | |
| Affected: | Air-In-Line (AIL) Sensor kits, part numbers 147083-102 and 49000221 |
| 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 AIL alarms that have occurred when no air is observed in the line. While the pump is infusing, the system may indicate that an AIL alarm has occurred when no air is in the line. In some cases, these false AIL alarms may be attributed to a faulty AIL sensor. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 9/3/2017 |
