Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
- Company
- Teleflex Medical Inc
- Recall Initiated
- January 9, 2020
- Posted
- February 7, 2020
- Terminated
- September 11, 2023
- Recall Number
- Z-1117-2020
- Quantity
- 338,928 (199,018 US and 139,910 OUS) for all products
- Firm Location
- Morrisville, NC
Reason for Recall
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.
Distribution
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
Lot / Code Info
Product Code 004551004; Lot Numbers 1812341, 1903341
Root Cause
Process control
Action Taken
Letters sent to customers/users to immediately discontinue use and quarantine any products with the affected product code and lot numbers and return them to the manufacturer.
More recalls by Teleflex Medical Inc
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile;
(2) Gibeck Humid-Vent 2S Flex DC, Product...
Apr 11, 2022
(1) Teleflex Flex tube, Product #20011, sterile;
(2) Teleflex Smooth-Flo Flex with Double Swivel, Pr...
Apr 11, 2022
5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing...
Feb 15, 2022