FDA Device recall Z-1294-2015
LeMaitre Vascular Tumescent Catheter Inversion (TCI) System
- FDA Device
- Class III
- terminated
- Published 2015-03-25
On 2015-03-25 the FDA classified a Class III recall of LeMaitre Vascular Tumescent Catheter Inversion (TCI) System by Lemaitre Vascular, citing mislabeled with an incorrect expiration date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1294-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-02-24 |
| Published | 2015-03-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Lemaitre Vascular |
| Distribution | CA, CO, KS, MN, UT, WA, WI |
Product
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
Reason
Mislabeled with an incorrect expiration date
Identifiers
| code_info | Lot Number: 61049252 Exp. Date: 2016-06 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1294-2015%22
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