FDAOctober 11, 2023device

Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to include: 1. AirFlow Adult Resuscitator REF #s: AF1140MB-M5, AF1140MB-D5, AF5142OB, AF5142MB, AF5142MB-D235, AF1142MBP, AF5142MBP, AF5140MB, AF5140MB-2, AF5140MB-D6, AF5140MB-F, AF1140M...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.

What to do

FDA enforcement status: Ongoing

Brands named

sunmed

UPCs

108894830758143088948307581810889483076606308894830766001088948307661330889483076617108894830758383088948307583210889483088074308894830880781088948308620930889483086203

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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