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FDAJuly 12, 2024device

RMU-2000 Automated Chest Compression Device

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

The hazard

Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death.

What to do

FDA enforcement status: Ongoing

Brands named

defibtech

UPCs

0081509802081210815098020819

Recall history

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

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RMU-2000 Automated Chest Compression Device — Recall Details · AllClear