Draeger Medical Recalls Ventstar Oxylog 3000 Pediatric Breathing Circuits
The FDA today released information on a Class I recall of Draeger Medical‘s VentStar Oxylog 3000 disposable pediatric patient circuits over issues with air leakage.
The federal watchdog labeled the recall as a Class I, the agency’s most serious classification of recall. Class 1 designations are used when there is a reasonable probability that product use could cause serious adverse health consequences or death.
The federal watchdog labeled the recall as a Class I, the agency’s most serious classification of recall. Class 1 designations are used when there is a reasonable probability that product use could cause serious adverse health consequences or death.