The Food and Drug Administration (FDA) has canceled the recall of superbug-linked scope cleaners, according to an article on the Fierce Healthcare website.
The FDA said that while hospitals can't use Custom Ultrasonics' System 83 Plus Automated Endoscope Reprocessors (AERs) to disinfect the duodenoscopes linked to superbug outbreaks, they could be used for other endoscopes.
Custom Ultrasonics is working with the FDA to resolve duodenoscope issues as quickly as possible, the company said.
The results of a Senate investigation published in January faulted regulators, hospitals and scope manufacturers along with Custom Ultrasonics for outbreaks.
ISSA Introduces Healthcare Platform to Advance Safer, Cleaner Patient Environments
Third-Party Tracking Settlement is a Compliance Wake-Up Call for Healthcare Facilities Managers