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Ventlab Corporation recalls Adult Resuscitator, Pro-5000 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressu
Recalled November 7, 2012 · FDA recall Z-0171-2013 · Ventlab
Hazard
Possible volume leakage through the inlet valve during compressions of the resuscitator bag. · FDA Class I
Units
14,602 total for all units
Sold at
Nationwide Distribution including IL, OH, NY and TN.
Description
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Product
Adult Resuscitator, Pro-5000 Series, Single Patient Use, 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.
Manufacturer(s)
Ventlab Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →