Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
AirFlow Resuscitator Recalled by Ventlab Corporation Due to Possible volume leakage through the inlet valve during...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ventlab Corporation directly.
Affected Products
AirFlow Resuscitator, Adult Resuscitator, AF1000 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 arrest.
Quantity: 14,602 total for all units
Why Was This Recalled?
Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ventlab Corporation
Ventlab Corporation has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report