Biotronik Inc Belos VR-T Implantable Cardioverter Defibrillator (ICD) with version A-K00.1.U/1 programmer software. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Belos VR-T Implantable Cardioverter Defibrillator (ICD) with version A-K00.1.U/1 programmer software.
Brand
Biotronik Inc
Lot Codes / Batch Numbers
Serial Numbers: 7814xxxx
Products Sold
Serial Numbers: 7814xxxx
Biotronik Inc is recalling Belos VR-T Implantable Cardioverter Defibrillator (ICD) with version A-K00.1.U/1 programmer software due to Potential for early depletion of Implantable Cardioverter Defibrillator battery.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for early depletion of Implantable Cardioverter Defibrillator battery.
Recommended Action
Per FDA guidance
Firm issued a letter dated September 24, 2003 recommending physicians schedule an immediate follow-up to reprogram the affected devices.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026