Home / Recalls / Medical Devices
TELEFLEX MEDICAL INC recalls Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Recalled February 19, 2020 · FDA recall Z-1117-2020 · TELEFLEX MEDICAL
Hazard
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth. · FDA Class II
Units
338,928 (199,018 US and 139,910 OUS) for all products
Sold at
Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218
Description
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Product
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Manufacturer(s)
TELEFLEX MEDICAL INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →