Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Recalled by ZOLL Circulation, Inc. Due to AutoPulse NXT Resuscitation System may not provide adequate...
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
Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (Catalog Number: 8700-001070-1) Software Version: Version 2.0.1 Product Description: The AutoPulse Resuscitation System Model 200 is an automated, portable, battery powered device that compresses the chest of an adult human as an adjunct to manual CPR. Component: N/A
Quantity: 91
Why Was This Recalled?
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
Where Was This Sold?
This product was distributed to 19 states: AL, CA, CT, FL, IL, KS, LA, MN, MO, MT, NM, NY, NC, ND, OH, OK, PA, TX, WI
About ZOLL Circulation, Inc.
ZOLL Circulation, Inc. has 31 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report