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

Recall Z-0608-2020 — HeartStart XL+ Defibrillator/Monitor, Model 861290

U.S. FDA — Device Enforcement · United States · 2019-10-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0608-2020
Date of alert
2019-10-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips North America, LLC
Product category
device
Product type
Devices
Reported risk: Device may fail to turn on or unexpectedly attempt to restart, rendering it unable to return to a ready for use state. Additionally, this issue may occur when the device is in standby mode, when attempting to power on to run a self-test. If this occurs, the device will indicate that it is not ready for use.
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.

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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.