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Philips North America LLC: Philips, HeartStart HS1 Home Defibrillator, Model #

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Customers were not notified of previous recalls associated with various defibrillator models.. Recalled by Philips North America LLC. Distribution: 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.. Classification (Class II — potential health risk). Affected lots/dates: Affected serial numbers for Model # 5068A: A10A-01936, A09J-02570, A04L-01521, A10H-04433, A09J-01944, A07H-03121, A08A. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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