Archive for the ‘Medical Device Recalls & Safety Notices’ category

Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AEDĀ® and ReviveR AEDTM

June 8, 2010

Defibtech, LLC, is initiating a voluntary recall of 5,418 DBP-2800 Battery Packs used in the Lifeline AEDĀ® and ReviveR AEDTM (semi-automatic external defibrillators). This recall affects all DBP- 2800 Battery Packs shipped prior to June 4, 2007. In rare instances, when the AED is used with an affected battery pack, the AED may falsely detect […]

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