Angiodynamics, Inc. AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012
Brand
Angiodynamics, Inc.
Lot Codes / Batch Numbers
Lot 5456490, UPN H787114030120
Products Sold
Lot 5456490; UPN H787114030120
Angiodynamics, Inc. is recalling AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Cat due to The affected product is properly labelled with an expiration date of March 31, 2022; but the RFID programmed expiration date is April-2014 which resul. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Customers were contacted via telephone on 6/27/19 directing them to stop using the affected product and segregate until receipt of written Recall Notification. Urgent Voluntary Medical Device Recall notification letters were sent to customers on July 2, 2019.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL, IN, MI, NJ, TN, TX, WI, DC
Page updated: Jan 10, 2026