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SunMed Holdings, LLC recalls Ventlab, LLC RescuMed manual resuscitators with integrated manometer, multiple accessory configurations to include: 1
Recalled November 29, 2023 · FDA recall Z-0364-2024 · SunMed Holdings
Hazard
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing. · FDA Class II
Units
N/A
Sold at
US Nationwide distribution including in the states of AR, AZ, CA¿CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, NC, ND, NH, NJ, NM, NV, NY, OH, SC, TN, TX, UT, VA, & WV.
Description
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
Product
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 REF #s: BVMB812, BVMB812-F, BVMB810, BVMB810-F, BVMB810S-F.
Manufacturer(s)
SunMed Holdings, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →