Device recall
Z-0049-2012: ArthroCare brand MiniMagnum Knotless Fixation Implant Device with Inserter…
FDA device recall · Class II · ArthroCare Corporation
Key facts
| Recall number (Z-number) | Z-0049-2012 |
|---|---|
| Recall event | 59978 |
| Product | ArthroCare brand MiniMagnum Knotless Fixation Implant Device with Inserter Handle Plus SpeedStitch Magnum Wire Suture Cartridge; Catalog Number: OM-6007; Product is manufactured and distributed by ArthroCare Corporation, Sunnyvale, CA The MiniMagnum Knotless Fixation Device is indicated for use in… |
| Product code | HWC |
| Recalling firm | ArthroCare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 24, 2011 |
| 510(k) numbers | K042584 |
| 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