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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 21 Results
510(K) Number: K012842
 
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Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT50... 1 07/03/2014 Ventlab LLC
Safe Spot Infant Resuscitator, SS3200 Series, Single Patient Use, Manufactured by: Ventlab Corporati... 1 11/01/2012 Ventlab Corporation
AirFlow, Small Adult Resuscitator, AF5000 Series, Single use, Manufactured by: Ventlab Corporation, ... 1 11/01/2012 Ventlab Corporation
AirFlow, Infant Resuscitator, AF3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 B... 1 11/01/2012 Ventlab Corporation
Ventlab Rescue Med Infant Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockv... 1 11/01/2012 Ventlab Corporation
Ventlab Premium Small Adult Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Moc... 1 11/01/2012 Ventlab Corporation
Ventlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Moc... 1 11/01/2012 Ventlab Corporation
Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitator... 1 11/01/2012 Ventlab Corporation
AirFlow Resuscitator, Adult Resuscitator, AF1000 Series, Single use, Manufactured by: Ventlab Corpor... 1 11/01/2012 Ventlab Corporation
Breath Tech, Safe Spot Infant Resuscitator, BT2000 Series, Single use, Manufactured by: Ventlab Corp... 1 11/01/2012 Ventlab Corporation
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