# FDA recall Z-2444-2019

> **Angiodynamics, Inc.** · Class II · device recall initiated 2019-06-27.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2444-2019
- **Recalling firm:** Angiodynamics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-27
- **Report date:** 2019-09-11
- **Termination date:** 2020-07-29

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2444-2019

## Citation

> AI Analytics. FDA recall Z-2444-2019. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2444-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*