Biotronik Inc Belos DR-T Implantable Cardioverter Defibrillator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Belos DR-T Implantable Cardioverter Defibrillator
Brand
Biotronik Inc
Lot Codes / Batch Numbers
Serial Numbers: 79640026, 79640028, 79640030, 79640031, 79640032, 79640033, 79640035, 79640037, 79640039, 79640044, 79640048, 79640049, 79640053, 79640058, 79640060, 79640062, 79640064, 79640065, 79640070, 79640078, 79640079, 79640080, 79640081, 79640082, 79640085, 79640086, 79640087, 79640088, 79640089, 79640091, 79640093, 79640094, 79640095, 79640097, 79640104, 79640116, 79640117, 79640121, 79640239, 79640247, 79640252, 79640323, 79640324.
Products Sold
Serial Numbers: 79640026, 79640028, 79640030, 79640031, 79640032, 79640033, 79640035, 79640037, 79640039, 79640044, 79640048, 79640049, 79640053, 79640058, 79640060, 79640062, 79640064, 79640065, 79640070, 79640078, 79640079, 79640080, 79640081, 79640082, 79640085, 79640086, 79640087, 79640088, 79640089, 79640091, 79640093, 79640094, 79640095, 79640097, 79640104, 79640116, 79640117, 79640121, 79640239, 79640247, 79640252, 79640323, 79640324.
Biotronik Inc is recalling Belos DR-T Implantable Cardioverter Defibrillator due to Potential extended charge time anomalies.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential extended charge time anomalies.
Recommended Action
Per FDA guidance
Firm issued a letter dated September 24, 2003 recommending physicians schedule an immediate follow-up with affected patients.
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