Device recall
Z-0625-2009: Stryker Vision 3 Flat Panel Shroud, Part #0682-000-414 (Individual Flat Panel…
FDA device recall · Class II · Stryker Communications Corp
Key facts
| Recall number (Z-number) | Z-0625-2009 |
|---|---|
| Recall event | 49568 |
| Product | Stryker Vision 3 Flat Panel Shroud, Part #0682-000-414 (Individual Flat Panel Shroud, Ver. 2, Reworked), 0682-000-415 (SV3 Shroud Retro Fit Kit) and 0682-000-416 (Flat Panel Retro Fit Kit); distributed by Stryker Communications, Flower Mound, TX 75028. The 0682-000-414 (FP Shroud version 2 reworked)… |
| Product code | FQO |
| Recalling firm | Stryker Communications Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 8, 2010 |
| FEI number | 3002975342 |
At a glance
- None 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