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FDASeptember 22, 2022device

AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

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

The hazard

Due to increase in Li-Ion Battery failures

What to do

FDA enforcement status: Ongoing

Brands named

zoll circulationzoll

Recall history

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

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