Device recall
Z-1860-2021: Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003…
FDA device recall · Class I · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-1860-2021 |
|---|---|
| Recall event | 87952 |
| Product | Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004, The angiographic guidewire components associated with this recall are manufactured with a requirement that further downstream processing (sterilization) is required. Indications for use for these components are… |
| Product code | NKQ |
| Recalling firm | Medtronic Vascular |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 5, 2023 |
| FEI number | 1220452 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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