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Facilities Must Stop Using Custom Ultrasonics' System To Reprocess Duodenoscopes, FDA Warns

Executive Summary

The US agency issued a safety communication Aug. 17 advising all health care facilities to stop using Custom Ultrasonics' System 83 Plus automated endoscope reprocessors to reprocess duodenoscopes, although facilities may continue to use the AERs to clean and sterilize other flexible endoscopes.

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