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All product recalls associated with BIOTRONIK Inc.
Total Recalls
37
Past Year
0
Class I (Serious)
0
Most Recent
Mar 2021
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
Timing Feature Error: An implementation error allows the usage of the V-V timing feature, which is not approved for use in the U.S.
Potential for device to not deliver full amount of energy
Potential for device to not deliver full amount of energy
Potential for device to not deliver full amount of energy
Potential for device to not deliver full amount of energy
Potential for early depletion of Implantable Cardioverter Defibrillator battery.
Potential extended charge time anomalies.
Potential extended charge time anomalies.
Potential extended charge time anomalies.
Potential extended charge time anomalies.
Potential for early depletion of Implantable Cardioverter Defibrillator battery.
Potential extended charge time anomalies
Potential extended charge time anomalies