Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21034 |
| Brand Name: | Medtronic - 8840 N'Vision |
| Model: | |
| Affected: | 8840 N'Vision |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Inc |
| Issue: | This is a follow up to the May 2013 communication regarding the SynchroMed II priming bolus function to inform you that the manufacturer is updating the Model 8870 software application card (to version BBU01) as well as the SynchroMed® Infusion System labeling to address the issue. The SynchroMed priming bolus function is intended to quickly advance drug from the pump reservoir to the catheter tip to allow for therapy initiation while the patient remains under medical supervision. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 24/1/2017 |
