Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1533-2025 — 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

U.S. FDA — Device Enforcement · United States · 2025-03-04 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1533-2025
Date of alert: 2025-03-04
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: ZOLL Circulation, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00849111003384

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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