Recall of the dual chamber C- and T-series pacemakers from Vitatron
2007.03.01
Product group Active implantable medical devices
Reference 00310/07
Vitatron has issued a recall due to possible software anomaly effecting dual chamber C- and T-series pacemakers.
Recall of the dual chamber C- and T-series pacemakers from Vitatron , Download_VeroeffentlichtAm_EN