Angiodynamics Inc. (Navilyst Medical Inc.): Medical Device Recall in 2019 - (Recall #: Z-0411-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151

Product Classification:

Class II

Date Initiated: October 2, 2019

Date Posted: November 27, 2019

Recall Number: Z-0411-2020

Event ID: 84072

Reason for Recall:

The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.

Status: Terminated

Product Quantity: 30

Code Information:

Lot 5476032

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated