On Nov. 13, 2015, the Food and Drug Administration ordered a recall of all Custom Ultrasonics AERs due to an increased risk of infection transmission. The AER is a machine/system that cleans and disinfects endoscopes between uses. If not properly cleaned, the endoscope can transmit a bacterial infection called carbapenem-resistant enterobacteriaceae (CRE). CRE is highly antibiotic-resistant, has a high mortality rate and must be diagnosed by culture.
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