Recall Z-1117-2020— TELEFLEX MEDICAL INC
Class II · Terminated
Class II FDA medical device recall by TELEFLEX MEDICAL INC, initiated 2020-01-09, terminated 2023-09-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System. Reason: 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..
- Recalling firm
- TELEFLEX MEDICAL INC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-01-09
- Terminated
- 2023-09-11
- Firm location
- Morrisville, NC, United States
Product description
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.