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Sun Med, LLC recalls STAT-Check MANUAL RESUSCITATOR / VENTILATOR, REF SC9200MBP-1
Recalled June 20, 2018 · FDA recall Z-2145-2018 · 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
76 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
STAT-Check MANUAL RESUSCITATOR / VENTILATOR, REF SC9200MBP-1
Manufacturer(s)
Sun Med, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →