Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13949 |
| Brand Name: | Hospira Plum A+ Infusion Pumps |
| Model: | Models: 11971, 11973, 12391, 20679, 12348, 12618, 20678, 11005 |
| Affected: | All serial numbers |
| Software version: | |
| Recalling Organisation: | Hospira NZ Ltd 58 Richard Pearse Drive Airport Oaks Mangere Auckland 2022 |
| Contact Information: | 04 384 7463 |
| Manufacturer: | Hospira Inc |
| Issue: | The door roller assembly on the Plum A+/A+3 infuser family of infusers has the potential to break which can lead to possible unrestricted flow and/or overdelivery during the removal of the IV administration set's cassette from the pump. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 3/4/2013 |
