LIFEPAK CR Plus Automated External Defibrillators (Physio-Control, Inc)

Date of Recall
2009-09-16

Recall Details
FDA 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.

Recall Comments

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