# FDA recall Z-0118-2023

> **ZOLL Circulation, Inc.** · Class II · device recall initiated 2022-09-22.

## Product

AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100.  used as an adjunct to manual CPR

## Reason for recall

Due to increase in Li-Ion Battery failures

## Distribution

U.S.: AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, RN, TX, UT, VA, VT, Virgin Islands, WA, WI, WV and WY.  O.U.S.: United Arab Emirates, Austria, Australia, Azerbaijan, Brazil, Belarus, Canada, Switzerland, China, Costa Rica, Germany, Denmark, Egypt, France, United Kingdom, Greece, Hong Kong, Croatia, Hungary, Israel, India, Iraq, Italy, Jordan, Japan, South Korea, Moldova, Mexico, Malaysia, Netherlands, Norway, Panama, Philippines, Poland, Qatar, Romania, Russian, Saudi Arabia, Singapore, Slovenia, Taiwan, and Vietnam.

## Key facts

- **Recall number:** Z-0118-2023
- **Recalling firm:** ZOLL Circulation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-22
- **Report date:** 2022-11-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Jose, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0118-2023

## Citation

> AI Analytics. FDA recall Z-0118-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0118-2023. Source: US FDA. Licensed CC0.

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