# FDA recall Z-0411-2020

> **Angiodynamics Inc. (Navilyst Medical Inc.)** · Class II · device recall initiated 2019-10-02.

## 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.

## Distribution

The products were distributed to the following US states:  LA, MA, OR, VA, and WA.

## Key facts

- **Recall number:** Z-0411-2020
- **Recalling firm:** Angiodynamics Inc. (Navilyst Medical Inc.)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-02
- **Report date:** 2019-11-27
- **Termination date:** 2020-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Glens Falls, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0411-2020

## Citation

> AI Analytics. FDA recall Z-0411-2020. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-0411-2020. Source: US FDA. Licensed CC0.

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