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Product Recalls & Refunds WA

Physio-Control, Inc.: LIFEPAK 20e REF 99507-000001 The AED mode is to be used

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

Recall reason: Incorrect keypad was incorrectly installed onto a defibrillator/monitor.. Recalled by Physio-Control, Inc.. Distribution: U.S.: WV O.U.S.: N/A. Classification (Class II — potential health risk). Affected lots/dates: Model/Catalog Number: 99507-000001 UDI-DI code: 00883873813751 Serial Number: 38289467. 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 WA
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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