Stryker Launches Voluntary Field Action for Specific Units of the LIFEPAK® 15 Monitor/Defibrillator

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Beef E. coli Outbreak investigation

The provider is notifying certain LIFEPAK 15 clients of an issue that can cause the device to lock up after a defibrillation shock is delivered. The lock-up condition is described as a sterile monitor screen with LED lights indicating power to the apparatus, but no response from the keypad and device works. A device in this state has the potential to delay delivery of treatment, and this delay in treatment has the potential to cause serious harm or death.



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