Device recall
Z-0510-2019: Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage…
FDA device recall · Class II · Numed Inc
Key facts
| Recall number (Z-number) | Z-0510-2019 |
|---|---|
| Recall event | 81460 |
| 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. |
| Product code | DQO |
| Recalling firm | Numed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 28, 2019 |
| 510(k) numbers | K952984 |
| FEI number | 1318694 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database