DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden ca...
FDA Recall #Z-1312-2023 — Class II — February 14, 2023
Product Description
DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest
Reason for Recall
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.
Recalling Firm
Defibtech, LLC — Guilford, CT
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
29 units
Distribution
US Nationwide distribution.
Code Information
UDI-DI: 00815098020003 Serial Numbers: 101702198 101702263 101702424 101702524 101702535 101702540 101702544 101702545 101703267 101703269 101703272 101703274 101703276 101703277 101703278 101703281 101703312 101703326 101703378 101703407 101703411 101703412 101703419 101703424 101703427 101703464 101703465 101703600 101704106
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated