FDAOctober 11, 2023device

Ventlab, LLC BreathTech manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. BreathTech Adult Resuscitator REF #s: BT5107F & BT5104P; 2. BreathTech Child Resuscitator REF #s: BT3030, BT3034, & BT3025; 3. BreathTech Infant Resuscitator REF #s: BT2415K, B...

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

108894830907873088948309078110889483102046308894831020401088948309783030889483097834108894830832463088948308324010889483083253308894830832571088948308633930889483086333

Recall history

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

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Ventlab, LLC BreathTech manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. BreathTech Adult Resuscitator REF #s: BT5107F & BT5104P; 2. BreathTech Child Resuscitator REF #s: BT3030, BT3034, & BT3025; 3. BreathTech Infant Resuscitator REF #s: BT2415K, B... — Recall Details · AllClear