Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22304 |
| Brand Name: | Infusion pumps - Syringe (Swiss) |
| Model: | |
| Affected: | Product codes with prefix (all variants): 8001, 8002, 8003,8004, and 8005 |
| 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 received a report regarding reoccurring PL3 alarms. A PL3 alarm is an internal malfunction error code, which will result in the pump stopping and alerting the user of an internal failure. If a pump displays a PL3 error message, the pump should be immediately removed from clinical use and sent for servicing by qualified service personnel. |
| Recall action type: | Alert |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/11/2017 |
