Device recall
Z-1952-2011: ArthroCare Opus SpeedLock Knotless Fixation Device; Catalog Number: OM-7500.
FDA device recall · Class II · ArthroCare Corporation
Key facts
| Recall number (Z-number) | Z-1952-2011 |
|---|---|
| Recall event | 57830 |
| Product | ArthroCare Opus SpeedLock Knotless Fixation Device; Catalog Number: OM-7500. |
| Product code | MBI |
| Recalling firm | ArthroCare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2011 |
| 510(k) numbers | K090615 |
| FEI number | 3010813691 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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