# FDA recall Z-1533-2025

> **ZOLL Circulation, Inc.** · Class I · device recall initiated 2025-03-04.

## Product

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

## Reason for recall

AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.

## Distribution

US: AL, CA, CT, FL, IL, KS, LA, MN, MO, MT, NC, ND, NM, NY, OH, OK< PA, TX, WI OUS: Canada, Hong Kong,

## Key facts

- **Recall number:** Z-1533-2025
- **Recalling firm:** ZOLL Circulation, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-04
- **Report date:** 2025-04-23

- **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-1533-2025

## Citation

> AI Analytics. FDA recall Z-1533-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1533-2025. Source: US FDA. Licensed CC0.

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