| Subject: | Class I Recall of LIFEPAK 15 Monitor and Defibrillator by Physio-Control Inc. |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 23 Apr 2010 - 10:00 am |
| Audience: Emergency medical personnel, consumers The Food and Drug Administration (FDA) has notified healthcare professionals of a Class I recall of LIFEPAK 15 Monitor/Defibrillator manufactured and distributed between March 26, 2009 and December 15, 2009. The device is being recalled because there is a potential for the device to unexpectedly: Power Off then On by itselfPower Off then NOT turn OnPower Off by itself requiring the operator to turn it back OnStay powered On and not allow itself... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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