Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29762 |
| Brand Name: | CN - Percept PC BrainSense B35200 |
| Model: | A610 Clinician Software Application |
| Affected: | |
| Software version: | 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081 |
| 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: | The manufacturer has identified an anomaly with the clinician programmer application (A610) when interrogating an Activa™ PC or Activa™ RC. In rare instances, this anomaly may present during a follow-up session if the patient was previously programmed with an A610 DBS Clinician Programmer Application Version v.2.0.x (2.0.4584, 2.0.4594, 2.0.4605, and 2.0.4630) and later that same Activa™ PC or Activa™ RC patient's device is interrogated with a clinician programmer tablet running A610 3.0.x |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/7/2022 |
