Device recall
Z-1454-2014: Alligator Retrieval Device (ARD). Used in the peripheral and neurovasculature…
FDA device recall · Class I · Micro Therapeutics Inc, Dba Ev3 Neurovascular
Key facts
| Recall number (Z-number) | Z-1454-2014 |
|---|---|
| Recall event | 67893 |
| Product | Alligator Retrieval Device (ARD). Used in the peripheral and neurovasculature for foreign body removal. |
| Product code | DQY |
| Recalling firm | Micro Therapeutics Inc, Dba Ev3 Neurovascular |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 31, 2014 |
| 510(k) numbers | K043580 |
| FEI number | 3004904811 |
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