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Pentax Medical Company recalls Video Duodenoscope
Recalled June 8, 2016 · FDA recall Z-1835-2016 · Pentax Medical
Hazard
Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae (CRE) infection at a medical facility. · FDA Class II
Units
423 units
Sold at
Nationwide
Description
Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae (CRE) infection at a medical facility.
Product
Video Duodenoscope
Manufacturer(s)
Pentax Medical Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →