Rusch Greenlite MAC 1 — Class II medical device recall Z-0705-2018
Terminated recall by Teleflex Medical, reported 2018-03-07. The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSC
| Recall number | Z-0705-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2017-01-10 |
| Classified | 2018-02-23 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2021-04-13 |
| Quantity | 2,140 units |
| Reason classes | labeling |
| Serial numbers | 1602312 |
| Model numbers | 004551001 |
Product
Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Reason for recall
The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.
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-0705-2018. 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.