Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26342 |
| Brand Name: | Alaris System Infusion Pumps_CFN San Diego |
| Model: | |
| Affected: | All software versions |
| Software version: | |
| Recalling Organisation: | Becton Dickinson Ltd Unit 4 / 110 Mays Road Onehunga Auckland 1061 |
| Contact Information: | 0800 572 468 |
| Manufacturer: | CareFusion 303 Inc |
| Brand Name: | Alaris System Infusion pump, syringe_CFN San Diego |
| Model: | |
| Affected: | All software versions |
| Software version: | |
| Recalling Organisation: | Becton Dickinson Ltd Unit 4 / 110 Mays Road Onehunga Auckland 1061 |
| Contact Information: | 0800 572 468 |
| Manufacturer: | CareFusion 303 Inc |
| Brand Name: | Alaris System EtCO2 |
| Model: | |
| Affected: | all software versions |
| 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 four hardware issues with BD Alaris systems. Overview of the Issue: The IUI connectors provide power and communication between PC Unit and modules of the Alaris System (PCU, LVP, Syringe, PCA, and EtC02 modules). Each module has a male and female IUI connector. A corroded or damaged IUI may result in interruption of communication and/or power between PC Unit and its connected modules. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/7/2020 |
