BRAEMAR Recalls
2 recalls on record · July 10, 2013 to July 10, 2013 · Medical Devices
July 10, 2013Medical DevicesFDA
BRAEMAR, INC. recalls Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01 used with ER920 Wireless Series Arrhythmia Even
Hazard: Braemar has recently became aware of a battery related incident that occurred with EWT battery packs that are used in a Braemer ER920W wireless event monitor and Fusion device. The event did not result in any patient related injury or present any clinical impact.
July 10, 2013Medical DevicesFDA
BRAEMAR, INC. recalls Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00 used with ER920 Wireless Series Arrhythmia Even
Hazard: Braemar Inc., became aware of a battery related incident that occurred with an Able battery pack being used in a Braemar ER920W wireless event monitor. The event did not result in any patient related injury or present any clinical impact.