Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic… — Class II medical device recall Z-1117-2020
Terminated recall by TELEFLEX MEDICAL INC, reported 2020-02-19, distributed nationwide. The products are being recalled due to reports of breakage broke at the point of a welded joint either prior t
| Recall number | Z-1117-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX MEDICAL INC, Morrisville, NC, United States |
| Recall initiated | 2020-01-09 |
| Classified | 2020-02-07 |
| Reported by FDA | 2020-02-19 |
| Terminated | 2023-09-11 |
| Distributed | Nationwide (US) |
| Reason classes | device malfunction |
| Lot numbers | 1812341, 1903341 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1117-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.