Class II — Numed Inc
| Recalling firm | NUMED, INC. |
|---|---|
| Registered facility | NUMED, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Instructions for Use booklets were not included on the outer pouch |
| Product | Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA06100 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. |
| Quantity | 100 units |
| Distribution | US distribution in the state of PA |
| Initiated | 2018-10-17 |
| Classified | 2018-11-28 |
| Terminated | 2019-01-28 |
| Recall number | Z-0511-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Numed Inc (Z-0511-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81460/
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