Skip to content
Recall Observatory FDA recall evidence

Device product

Ventlab Premium Small Adult Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.

Z-0178-2013

July 11, 2012

Class I

Product summary

Firm
Ventlab Corporation
Event
Event 63347
Status
Terminated
Classification
Class I
Quantity
14,602 total for all units
Official record key
device-enforcement:Z-0178-2013

Official wording

Reason: Possible volume leakage through the inlet valve during compressions of the resuscitator bag.

Code information: Product Code: VN500MX, Lot #102194.

Distribution pattern: Nationwide Distribution including IL, OH, NY and TN.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Possible volume leakage through the inlet valve during compressions of the resuscitator bag.