LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with… — Class II medical device recall Z-1445-2017
Terminated recall by LeMaitre Vascular, Inc., reported 2017-03-22, distributed nationwide. The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
| Recall number | Z-1445-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LeMaitre Vascular, Inc., Burlington, MA, United States |
| Recall initiated | 2017-02-07 |
| Classified | 2017-03-13 |
| Reported by FDA | 2017-03-22 |
| Terminated | 2019-09-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, BE, CH, DE, ES, FR, GB, IT, LU, MA, SA, SG |
| Quantity | 250 |
| Reason classes | labeling, sterility |
| Lot numbers | 2018-09, 2018-12, 2019-03, 2019-05, RED1747, RED1754, RED1763, RED1770 |
| Model numbers | E2400-53 |
Product
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53
Reason for recall
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
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-1445-2017. 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.