Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21796 |
| Brand Name: | CRDM - MyCarelink Patient Monitor |
| Model: | |
| Affected: | Model 25000 |
| 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 |
| Brand Name: | CRHF - MyCareLink Patient Monitor Model 24950 |
| Model: | |
| Affected: | Model 24950 |
| 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: | If a patient has multiple devices, there are potential impacts on the ability to remotely monitor that patient's heart devices. These potential impacts could lead to missed CareAlert™ notifications or device reports. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/8/2017 |
