FDAOctober 11, 2023device

Ventlab, LLC RescuMed manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. RescuMed Adult Resuscitator REF #s: BVM510-F, BVMB510-10, BVMB510-F, BVMB510S-F; 2. RescuMed Infant Resuscitator REF #s: BVMB710 & BVMB710-F; 3. RescuMed Pediatric Resuscitator R...

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

10889483164266308894831846801088948316475430889483164758108894831647853088948316478910889483164761308894831647651088948316960530889483169609108894831646860889483164680

Recall history

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

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Ventlab, LLC RescuMed manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. RescuMed Adult Resuscitator REF #s: BVM510-F, BVMB510-10, BVMB510-F, BVMB510S-F; 2. RescuMed Infant Resuscitator REF #s: BVMB710 & BVMB710-F; 3. RescuMed Pediatric Resuscitator R... — Recall Details · AllClear