FDAApril 27, 2020device

DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN DDU-E2450FR DDU-E2450TH Cat. No. DCF-A2460EN DCF-A2463EN DCF-E2460DE DCF-E2460EN DCF-E2460FR DCF-E2460TH UDI 00815098020287, 00815098020317 Automated External Defibrillators (AED) are indicated for use on victims of sudden ca...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.

What to do

FDA enforcement status: Terminated

Brands named

defibtech

UPCs

0081509802028700815098020317

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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