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Zoll Circulation, Inc. recalls AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automati
Recalled January 16, 2013 · FDA recall Z-0658-2013 · Zoll Circulation
Hazard
Complaints associated with an unexpected stop in AutoPulse compressions. · FDA Class II
Units
3881 in US, 1846 ROW.
Sold at
Worldwide distribution.
Description
Complaints associated with an unexpected stop in AutoPulse compressions.
Product
AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor is intended to be used as an adjunct to manual CPR, on adult patients only, in cases of clinical death as defined by lack of spontaneous breathing and pulse.
Manufacturer(s)
Zoll Circulation, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →