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Sun Med, LLC recalls MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE AND 7 FT. OXYGEN TUBING, RE
Recalled June 20, 2018 · FDA recall Z-2156-2018 · Sun Med
Hazard
There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use. This may impact air delivery to the patient. · FDA Class II
Units
361 cases
Sold at
IL & OH distributors
Description
There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use. This may impact air delivery to the patient.
Product
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1126FP
Manufacturer(s)
Sun Med, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →