Ventlab Recalls
14 recalls on record · November 7, 2012 to June 8, 2016 · Medical Devices
Recalls by year
12
14
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 8, 2016Medical DevicesFDA
Ventlab LLC recalls STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon dioxide gas analyzer Intended for use in v
Hazard: Stat-check CO2 indicators are non-functional. The indicator is yellow when not in use and should be purple when not in use. The yellow indicates a 5% CO2 level, cardiac massage and ventiliation being performed correctly. The color will not change during use and will not be an indicator of CO2 level or improper performance of cardiac message and ventilation.
July 9, 2014Medical DevicesFDA
Ventlab LLC recalls Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT5000, BVM700, CPRM1000
Hazard: The pop-off valve in the defective devices remain open and a squeeze of the bag may not generate enough force to force the duck bill valve open and therefore no air will be delivered to the victim.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls AirFlow, Small Adult Resuscitator, AF5000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Moc
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls AirFlow, Infant Resuscitator, AF3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockvill
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Ventlab Rescue Med Infant Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. T
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Ventlab Premium Small Adult Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028.
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Ventlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028.
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitators with optional buil
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls AirFlow Resuscitator, Adult Resuscitator, AF1000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Dri
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Breath Tech, Safe Spot Infant Resuscitator, BT2000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce D
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls V*Care Resuscitator Infant Resuscitator, VN 3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Dri
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Stat-Check Resuscitator, Adult Manual Emergency Resuscitator with A.C.E. /Stat-Check CO2 Indicator, SC 9000 Series, Sing
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Adult Resuscitator, Pro-5000 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressu
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
November 7, 2012Medical DevicesFDA
Ventlab Corporation recalls Safe Spot Infant Resuscitator, SS3200 Series, Single Patient Use, Manufactured by: Ventlab Corporation, 155 Boyce Drive,
Hazard: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.