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.
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📍Recalling firmAngiodynamics, Inc.603 Queensbury Ave · Queensbury, NY 12804-7619
✎ GovInfoNow plain-language explainer
Angiodynamics is recalling a specific VenaCure EVLT procedure kit because its RFID chip shows an outdated expiration date (April 2014) that causes it to display an error when connected to laser systems. This prevents the kit from being used properly, so affected users should stop using it. Read more at govinfonow.com/recall/67577-angiodynamics-venacure-evlt-kit-rfid-expiration-error-prevents-use.
“Angiodynamics VenaCure EVLT Kit: RFID Expiration Error Prevents Use.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/67577-angiodynamics-venacure-evlt-kit-rfid-expiration-error-prevents-use. Based on FDA recall #Z-2444-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2444-2019%22&limit=1).
Angiodynamics, Inc. voluntarily recalled the AngioDynamics VenaCure EVLT NeverTouch Procedure Kit on June 27, 2019, according to the FDA. The device's RFID programmed expiration date is April 2014, causing an error message that prevents use.
The product is labeled with an expiration date of March 31, 2022; however, the RFID programmed expiration date is April-2014. This discrepancy results in an error message when connected to the laser source and prevents the product from being used.
Context
GovInfoNow's records show Angiodynamics, Inc. has had 18 other recalls since June 5, 2017. Recent brand recalls include a March 3, 2026 recall for a Soft-Vu Catheter and a Feb. 4, 2025 recall for an IsoLoc Prostate Balloon Kit. Other recent recalls of similar products include an Aug. 24, 2026 Expressaire Disposable Tourniquet Cuff recall and a Dec. 18, 2025 Vascutek Gelsoft Plus and Gelweave devices recall.
How to tell if you have this one
Check for the Catalog Number 11403012 on the kit. The specific model is the 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG. This product was sold with Lot 5456490 and UPN H787114030120.
Brand
Angiodynamics
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the Catalog Number 11403012 on the kit's label to confirm it is affected.
Where it went and when
Where it was distributed
Distributed in 7 states and D.C..
Listed by the agency
Not listed
FDA distribution: “The products were distributed to the following US states: DC, IL, IN, MI, NJ, TN, TX, and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: District of Columbia, Illinois, Indiana, Michigan, New Jersey, Tennessee, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2444-2019 (June 27, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2444-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.