| Subject: | Class I Recall of Defibtech Lifeline and ReviveR Automated External Defibrillators |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 8 Mar 2007 - 12:00 am |
| Defibtech, LLC, has initiated a voluntary worldwide recall of the Lifeline AED® and ReviveR AEDTM (semi-automatic external defibrillators). This recall affects all Lifeline and ReviveR AEDs with software versions 2.002 and earlier.
The self-test software for these devices may allow a self-test to clear a previously detected low battery condition. If this situation occurs, the operator may be unaware of the low battery, and the device may be unable to deliver a defibrillation shock, which... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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