Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 — Class II medical device recall Z-2732-2020
Terminated recall by TELEFLEX MEDICAL INC, reported 2020-08-05, distributed nationwide. Breaking at the point of a welded joint
| Recall number | Z-2732-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX MEDICAL INC, Morrisville, NC, United States |
| Recall initiated | 2020-07-06 |
| Classified | 2020-07-28 |
| Reported by FDA | 2020-08-05 |
| Terminated | 2023-08-31 |
| Distributed | Nationwide (US) |
| Quantity | 29,740 units |
| UPC / GTIN / UDI-DI | 07290102156443 |
| Lot numbers | 1811351, 1812351, 1901351, 1903351, 1904351, 1905351, 1906351, 1907351, 1908351, 1909351 |
Product
Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
Reason for recall
Breaking at the point of a welded joint
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-2732-2020. 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.