FDA Device recall Z-1117-2020
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-1117-2020 |
| 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 004551004; Lot Numbers 1812341, 1903341 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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FDA Device · Class I · 2022-02-23 · Teleflex Medical - Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-…
FDA Device · Class I · 2022-02-23 · Teleflex Medical
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1117-2020%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.