Starburst Talon Semi-Flex Electrosurgical Device — Class II medical device recall Z-0411-2020
Terminated recall by Angiodynamics Inc. (Navilyst Medical Inc.), reported 2019-11-27, distributed in LA, MA, OR, VA, WA. The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.
| Recall number | Z-0411-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics Inc. (Navilyst Medical Inc.), Glens Falls, NY, United States |
| Recall initiated | 2019-10-02 |
| Classified | 2019-11-15 |
| Reported by FDA | 2019-11-27 |
| Terminated | 2020-07-29 |
| Distributed | LA, MA, OR, VA, WA |
| Quantity | 30 |
| Lot numbers | 5476032 |
| Model numbers | H7877001026151, H7877001028451 |
Product
Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151
Reason for recall
The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.
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-0411-2020. 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.