Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25026 |
| Brand Name: | Alaris System Infusion Pumps_CFN San Diego |
| Model: | Pump Module which all bezels manufactured between April 2011 and June 2017. |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Becton Dickinson Ltd Unit 4 / 110 Mays Road Onehunga Auckland 1061 |
| Contact Information: | 0800 572 468 |
| Manufacturer: | CareFusion 303 Inc |
| Issue: | The manufacturer has identified an issue with the Alaris pump module, manufactured between April 2011 and June 2017. All the bezels were manufactured with a specific type of plastic, called FR-110. |
| Recall action type: | Correction |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 27/8/2019 |
