FDA Device recall Z-1116-2020
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
- FDA Device
- Class II
- terminated
- Published 2020-02-19
On 2020-02-19 the FDA classified a Class II recall of Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System by Teleflex Medical, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1116-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-01-09 |
| Published | 2020-02-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Teleflex Medical |
| Distribution | US |
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.
Identifiers
| code_info | Product Code 004551003; Lot Numbers 1811331, 1902331, 1904331 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1116-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.