Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System Recalled by LeMaitre Vascular, Inc. Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact LeMaitre Vascular, Inc. directly.
Affected Products
LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System is intended to provide a system to the removal of an incompetent greater saphenous vein. Catalog Number: 7210023, lot #61049252
Quantity: 54 units
Why Was This Recalled?
Mislabeled with an incorrect expiration date
Where Was This Sold?
This product was distributed to 7 states: CA, CO, KS, MN, UT, WA, WI
About LeMaitre Vascular, Inc.
LeMaitre Vascular, Inc. has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report