Device recall
Z-1223-2020: Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil…
FDA device recall · Class II · Microvention, Inc.
Key facts
| Recall number (Z-number) | Z-1223-2020 |
|---|---|
| Recall event | 84585 |
| Product | Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 45-450820, and… |
| Product code | KRD |
| Recalling firm | Microvention, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2021 |
| 510(k) numbers | K151358 |
| FEI number | 3003523199 |
At a glance
- 1–9 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