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Philips North America, LLC recalls Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by qualif
Recalled June 3, 2020 · FDA recall Z-2137-2020 · Philips North America
Hazard
HeartStart XL MonitorlDefibrillators may not have been included in prior field actions and received required corrections · FDA Class II
Units
130 units (US 126; OUS 4)
Sold at
Worldwide distribution - US Nationwide distribution including in the states of KY, MA, ND, NY and the countries of United Kingdom, Bahrain.
Description
HeartStart XL MonitorlDefibrillators may not have been included in prior field actions and received required corrections
Product
Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac life support, or defibrillation
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →