Angiodynamics, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2444-2019)

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:

AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012

Product Classification:

Class II

Date Initiated: June 27, 2019

Date Posted: September 11, 2019

Recall Number: Z-2444-2019

Event ID: 83334

Reason for Recall:

The affected product is properly labelled with an expiration date of March 31, 2022; but the RFID programmed expiration date is April-2014 which results in an error message when connected to the laser source and prevents the product from being used.

Status: Terminated

Product Quantity: 109

Code Information:

Lot 5456490; UPN H787114030120

Distribution Pattern:

The products were distributed to the following US states: DC, IL, IN, MI, NJ, TN, TX, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated