FDAAugust 8, 2018device
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The recall is being initiated due to incorrect age range labeling (8+ yrs) on the foil packaging for infant/child pad cartridges. The infant/child pad cartridge is designed for use with the defibrillator An Infant/Child pad cartridge should not be used on an adult because it delivers lower energy (50 J vs 150 J) than the Adult pads cartridge and may therefore not be effective on an adult.
What to do
FDA enforcement status: Terminated
Brands named
philips north americaphilipsphilips north
UPCs
00884838023758
Recall history
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