Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model Recalled by ZOLL Circulation, Inc. Due to Due to increase in Li-Ion Battery failures
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 Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR
Quantity: 6,353 batteries
Why Was This Recalled?
Due to increase in Li-Ion Battery failures
Where Was This Sold?
This product was distributed to 46 states: AL, AK, AZ, AR, CA, CO, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, TX, UT, VT, VA, WA, WV, WI, WY
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