FDAOctober 27, 2017device

LIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.

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

The hazard

The infant artwork on the product instructs incorrect pad placement. Also, the artwork is missing the Type BF Patient connection and High Voltage Warning symbols.

What to do

FDA enforcement status: Terminated

Brands named

physio controlphysiophysio control

UPCs

11101000016

Recall history

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

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