Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23440 |
| Brand Name: | Alaris Plus Syringe Pumps_BD Swiss |
| Model: | (all variants): 8001, 8002, 8003, 8004, 8005, 8007 |
| Affected: | |
| Software version: | |
| Recalling Organisation: | CareFusion New Zealand 313 Limited Unit 4 / 110 Mays Road Onehunga AUCKLAND 1061 |
| Contact Information: | 0508 422 734 |
| Manufacturer: | BD Switzerland Sarl |
| Brand Name: | Alaris Plus Enteral Syringe Pump_IIa |
| Model: | 8002ENT, 8007ENT |
| Affected: | |
| Software version: | |
| Recalling Organisation: | CareFusion New Zealand 313 Limited Unit 4 / 110 Mays Road Onehunga AUCKLAND 1061 |
| Contact Information: | 0508 422 734 |
| Manufacturer: | BD Switzerland Sarl |
| Issue: | The manufacturer has identified that the gripper plate actuating spring (S5), can break and may prevent the gripper fingers from securing the syringe plunger within the plunger holder mechanism which causes a small gap between the syringe plunger flange and the syringe drive mechanism |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/8/2018 |
