Published on
December 20, 2019
- 15:32 GMT
LivaNova Recalls VNS Therapy SenTiva Generator Due to Reset Error
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Recalled Product(s): VNS Therapy SenTiva Generator System Model Number: 1000 Distribution Dates: …
Distribution channels:
Healthcare & Pharmaceuticals Industry
