FDA Announces Recall from Zoll Circulation

Zoll has announced a recall of its Model 200 Autopulse NXT Platform due to a failure code which indicates an error in compression depth. This may lead to incorrect compression depth or failure to compress.

Zoll advises immediately discontinuing use of the device if you possess one and to contact ZOLL Circulation, Inc. at 408-541-2140.

Further details can be found from Zoll Circulation or the FDA:

https://www.fda.gov/medical-devices/medical-device-recalls/resuscitation-system-recall-zoll-circulation-inc-recalls-autopulse-nxt-resuscitation-system-due?utm_medium=email&utm_source=govdelivery