Defibtech, LLC: DDU-100 Lifeline Automated External Defibrillator
Recall reason: A component of a sub-assembly used in the affected AEDs had not undergone durability and reliability testing, and if a malfunction occurs, therefore the device could fail to deliver therapy.. Recalled by Defibtech, LLC. Distribution: US Nationwide distribution.. Classification (Class II — potential health risk). Affected lots/dates: UDI-DI: 00815098020003 Serial Numbers: 101702198 101702263 101702424 101702524 101702535 101702540 101702544 101702545 1. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.
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