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

Recall Z-0658-2013 — AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor is intended to be used as an adjunct to manual CPR, on adult patients only, in cases of clinical death as defined by lack of spontaneous breathing and

U.S. FDA — Device Enforcement · United States · 2012-08-08 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0658-2013
Date of alert: 2012-08-08
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zoll Circulation, Inc.
Product category: device
Product type: Devices

Reported risk: Complaints associated with an unexpected stop in AutoPulse compressions.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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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