Device recall
Z-3253-2018: Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35
FDA device recall · Class III · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-3253-2018 |
|---|---|
| Recall event | 80919 |
| Product | Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35 |
| Product code | DQO |
| Recalling firm | Medtronic Vascular |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 7, 2021 |
| 510(k) numbers | K161287 |
| FEI number | 1220452 |
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