LeMaitre Vascular Tumescent Catheter Inversion — Class III medical device recall Z-1294-2015
Terminated recall by LeMaitre Vascular, Inc., reported 2015-03-25, distributed in CA, CO, KS, MN, UT, WA, WI. Mislabeled with an incorrect expiration date
| Recall number | Z-1294-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LeMaitre Vascular, Inc., Burlington, MA, United States |
| Recall initiated | 2015-02-24 |
| Classified | 2015-03-18 |
| Reported by FDA | 2015-03-25 |
| Terminated | 2015-05-21 |
| Distributed | CA, CO, KS, MN, UT, WA, WI |
| Quantity | 54 units |
| Reason classes | labeling |
| Lot numbers | 2016-06, 61049252 |
| Model numbers | 7210023 |
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 for recall
Mislabeled with an incorrect expiration date
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1294-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.