Solia S 53
Received Jul 31, 2026 · Event occurred Apr 10, 2026
Report 1028232-2026-03484 · MDR key 50094136
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
Male
- Unspecified Infection
Narrative
Additional Manufacturer Narrative
Combination Product: YES.An infection was observed following the implantation of this BIOTRONIK device. The sterilization process was investigated. The validated process assures that all sterilization parameters, such as gas concentration, temperature, humidity, etc., are within its specified ranges for each distributed device.Additionally, an analysis of validated microbiological indicators is performed after every sterilization procedure as evidence of successful completion of the sterilization process.Review of the BIOTRONIK complaint database did not reveal any changes regarding the trend for this type of incident.In summary, the infection was not device related.
Description of Event or Problem
System was explanted due to infection. Should additional information be received, this file will be updated.