Device recall
Z-0190-2007: Zimmer Spine ST360 Distal Thread Reduction Guide Pins, Part number: 07.00684.00…
FDA device recall · Class II · Zimmer Spine, Inc.
Key facts
| Recall number (Z-number) | Z-0190-2007 |
|---|---|
| Recall event | 36549 |
| Product | Zimmer Spine ST360 Distal Thread Reduction Guide Pins, Part number: 07.00684.00. Non-Sterile. Zimmer Spine, Inc., 7375 Bush Lake Road, Minneapolis, MN 55439 U.S.A. The Distal Thread Reduction Guide Pin is a reusable instrument that is part of a set of instruments used to perform reduction surgeries… |
| Product code | KWP |
| Recalling firm | Zimmer Spine, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2007 |
| 510(k) numbers | K022374, K041925 |
| FEI number | 1000115775 |
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