Device recall
Z-0401-2011: Millar Disposable Angiographic Catheter (Left Heart), manufactured for Millar…
FDA device recall · Class II · Millar Instruments, Inc
Key facts
| Recall number (Z-number) | Z-0401-2011 |
|---|---|
| Recall event | 57015 |
| Product | Millar Disposable Angiographic Catheter (Left Heart), manufactured for Millar Instruments, Inc 6001-A Gulf Freeway, Houston, Texas 77023 |
| Product code | DQO |
| Recalling firm | Millar Instruments, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 15, 2011 |
| 510(k) numbers | K952773, K993694 |
| FEI number | 1625382 |
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