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Olympus Corporation of the Americas recalls Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
Recalled September 6, 2023 · FDA recall Z-2495-2023 · Olympus Corporation of the Americas
Hazard
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large. · FDA Class II
Units
1859 units
Sold at
US Nationwide distribution.
Description
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Product
Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →