Device recall
Z-2238-2023: FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511…
FDA device recall · Class II · MICROVENTION INC.
Key facts
| Recall number (Z-number) | Z-2238-2023 |
|---|---|
| Recall event | 92580 |
| Product | FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA, FRED3524, FRED3524-CA, FRED3524-PMA, FRED3536-CA, FRED3536-PMA, FRED4007-PMA, FRED4012-CA, FRED4012-PMA, FRED4017-PMA, FRED4026, FRED4026-PMA, FRED4038-PMA, FRED4508, FRED4508-PMA… |
| Product code | OUT |
| Recalling firm | MICROVENTION INC. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3013556777 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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