Olympus Corporation of the Americas recalls Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
Recalled Product
Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
Hazard / Issue
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 04953170340369, 04953170288661, & 04953170288630; All Serial Numbers.
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