Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AutoPulse Resuscitation System Model 100 Recalled by Zoll Circulation, Inc. Due to Complaints associated with an unexpected stop in AutoPulse...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zoll Circulation, Inc. directly.
Affected Products
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.
Quantity: 3881 in US, 1846 ROW.
Why Was This Recalled?
Complaints associated with an unexpected stop in AutoPulse compressions.
Where Was This Sold?
Worldwide distribution.
About Zoll Circulation, Inc.
Zoll Circulation, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report