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Philips North America LLC recalls Philips, HeartStart FRx + Defibrillator, Model # Model #s: 861304
Recalled October 20, 2021 · FDA recall Z-0079-2022 · Philips North America
Hazard
Customers were not notified of previous recalls associated with various defibrillator models. · FDA Class II
Units
6 units
Sold at
U.S.: CA, CT, FL, GA, IN, MI, MO, NJ, NY, OH, TX, and WA. International distribution in the countries of Australia, Canada, France, Germany, Japan, Norway, Switzerland.
Description
Customers were not notified of previous recalls associated with various defibrillator models.
Product
Philips, HeartStart FRx + Defibrillator, Model # Model #s: 861304
Manufacturer(s)
Philips North America LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →