Multi-Track Angiographic Catheter — Class II medical device recall Z-0510-2019
Terminated recall by Numed Inc, reported 2018-12-05. Instructions for Use booklets were not included on the outer pouch
| Recall number | Z-0510-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Numed Inc, Hopkinton, NY, United States |
| Recall initiated | 2018-10-17 |
| Classified | 2018-11-28 |
| Reported by FDA | 2018-12-05 |
| Terminated | 2019-01-28 |
| Quantity | 100 units |
| UPC / GTIN / UDI-DI | 04046964312700 |
| Lot numbers | 5MT-1264, 5MT-1265 |
| Expiration dates | 2023-09-30 |
Product
Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for injection of contrast medium and pressure measurement in any chamber or vessel.
Reason for recall
Instructions for Use booklets were not included on the outer 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-0510-2019. 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.