Home » FDA Issues MedWatch for Device Sterilizer
FDA Issues MedWatch for Device Sterilizer
Reports of healthcare providers being burned following exposure to a sterilant solution have led to an FDA MedWatch on Steris’ System 1 (SS1) processor
used to sterilize devices. The agency attributes the adverse events to recent modifications to the SS1 processor that were not cleared by the FDA. It advises
healthcare providers to find alternatives to the SS1 as soon as possible.
Upcoming Events
-
23Apr
-
25Apr
-
07May
-
14May
-
30May