medical Class II Updated 2023-09-06

Olympus Corporation of the Americas recalls Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-T

Recalled Product

Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2.

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: 04953170407260, 04953170407208, and 04953170407147; All Serial Numbers.
View official government recall

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