ClearanceBrief
Recall Z-0172-2013 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

Ventlab Corporation

Stat-Check Resuscitator, Adult Manual Emergency Resuscitator with A.C.E. /Stat-Check CO2 Indicator, SC 9000 Series, Single use, 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 arres

DateNov 1, 2012 (initiated Jul 11, 2012)
StatusTerminated
ReasonPossible volume leakage through the inlet valve during compressions of the resuscitator bag.
Root causeComponent design/selection
ActionVentLab Corporation sent an Attention: Recall Notification letter dated July 10, 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory for the affected product, complete and return the enclosed response form by fax to 336-753-5002, indicating whether or not their facility has any of the affected product. Customers can also scan and email the response form to CSR@Ventlab.com. For questions regarding this recall call 336-753-5000.
Quantity14,602 total for all units
DistributionNationwide Distribution including IL, OH, NY and TN.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K982215MANUAL RESUSCITATOR WITH ACE
Medical Marketing Concepts, Sep 18, 1998