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Recall Observatory FDA recall evidence

Device product

Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00 used with ER920 Wireless Series Arrhythmia Event Recorder. Non-rechargeable disposable battery pack.

Z-1645-2013

May 02, 2011

Class II

Product summary

Firm
BRAEMAR, INC.
Event
Event 65423
Status
Terminated
Classification
Class II
Quantity
10,785 packs
Official record key
device-enforcement:Z-1645-2013

Official wording

Reason: 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.

Code information: n/a

Distribution pattern: Nationwide Distribution including FL, IL, MD, MN, NY, OH, PA, SC, TN, and TX.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.