| Subject: | FDA Announces for Class I Recall for LIFEPAK CR Plus Automated External Defibrillators |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 16 Sep 2009 - 12:00 pm |
| Audience: Emergency medical personnel, consumers The Food and Drug Administration (FDA) has notified healthcare professionals of a Class I recall of certain LIFEPAK CR Plus Automated External Defibrillators (AED) manufactured and distributed from July 9, 2008 through August 19, 2008. An extremely humid environment may cause the affected devices to improperly analyze the heart rhythm and may cause the device to delay or fail to deliver therapy.Please follow the link below to review the complete... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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