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Philips Medical Systems, Inc. recalls Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Recalled April 16, 2014 · FDA recall Z-1439-2014 · Philips Medical Systems
Hazard
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy · FDA Class II
Units
19 units
Sold at
Worldwide Distribution - US Distribution including the states of IN and WA., and the countries of : CHINA FRANCE GERMANY ITALY MALAYSIA PANAMA SAUDI ARABIA TURKEY and UNITED KINGDOM.
Description
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy
Product
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Manufacturer(s)
Philips Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →