Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21122 |
| Brand Name: | Alaris PK plus Infusion pumps - Syringe |
| Model: | |
| Affected: | Alaris™ PK plus Syringe Pump (model 8005TIG01) |
| 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 identified a potential risk with Alaris™ PK plus Syringe Pump (model 8005TIG01) whereby the Near End of Infusion (NEOI) audible alarm may not be heard or recognised by the clinician operating the pump. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/2/2017 |
