Angiodynamics recalls VenaCure EVLT NeverTouch Procedure Kit due to RFID expiration date error causing product incompatibility with laser systems.
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.
Angiodynamics is recalling a specific VenaCure EVLT procedure kit because its RFID chip shows an outdated expiration date (April 2014) that causes it to display an error when connected to laser systems.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.
The kit's RFID chip has an incorrect expiration date set to April 2014 instead of the actual March 2022 expiration. When connected to laser systems, this causes an error message that prevents the product from functioning properly.
Users of the Angiodynamics VenaCure EVLT NeverTouch Procedure Kit with Catalog Number 11403012 are affected. Medical professionals using this kit for vein treatments are most at risk due to potential incompatibility with laser systems.
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.
Look for the Catalog Number 11403012 on the kit's label to confirm it is affected.
The kit's RFID chip shows an incorrect expiration date (April 2014) that causes an error message when connected to laser systems, preventing proper use.
Check for the Catalog Number 11403012 on the kit's label. The specific model is the 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG with Lot 5456490 and UPN H787114030120.
The recall record does not specify a remedy, so affected users should contact Angiodynamics directly for guidance.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2444-2019 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2444-2019 from Angiodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
