Ventlab Corporation: Medical Device Recall in 2012 - (Recall #: Z-0177-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Ventlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028.

Product Classification:

Class I

Date Initiated: July 11, 2012

Date Posted: November 7, 2012

Recall Number: Z-0177-2013

Event ID: 63347

Reason for Recall:

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

Status: Terminated

Product Quantity: 14,602 total for all units

Code Information:

Product Code: VN4100OB, Lot #102015.

Distribution Pattern:

Nationwide Distribution including IL, OH, NY and TN.

Voluntary or Mandated:

Voluntary: Firm initiated