Device recall
Z-0268-2014: ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J…
FDA device recall · Class I · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-0268-2014 |
|---|---|
| Recall event | 66567 |
| Product | ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZRXT180S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral vasculature, and may be… |
| Product code | DQT |
| Recalling firm | Medtronic Vascular |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 15, 2014 |
| 510(k) numbers | K983927 |
| FEI number | 1220452 |
At a glance
- 1–9 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