AngioDynamics VenaCure EVLT NeverTouch Procedure Kit — Class II medical device recall Z-2444-2019
Terminated recall by Angiodynamics, Inc., reported 2019-09-11, distributed in DC, IL, IN, MI, NJ, TN, TX, WI. The affected product is properly labelled with an expiration date of March 31, 2022; but the RFID programmed e
| Recall number | Z-2444-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Inc., Queensbury, NY, United States |
| Recall initiated | 2019-06-27 |
| Classified | 2019-08-30 |
| Reported by FDA | 2019-09-11 |
| Terminated | 2020-07-29 |
| Distributed | DC, IL, IN, MI, NJ, TN, TX, WI |
| Quantity | 109 |
| Lot numbers | 5456490, H787114030120 |
| Model numbers | 11403012 |
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.
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-2444-2019. 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.