Device recall
Z-1043-05: ArthoCare Caps-Lock Cannula, polypropylene 70 mm cannula sterile, in double…
FDA device recall · Class II · ArthroCare Corporation
Key facts
| Recall number (Z-number) | Z-1043-05 |
|---|---|
| Recall event | 32688 |
| Product | ArthoCare Caps-Lock Cannula, polypropylene 70 mm cannula sterile, in double pouch, 10 pouches per chipboard box, lot code 1905. |
| Product code | GEA |
| Recalling firm | ArthroCare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 24, 2006 |
| FEI number | 3010813691 |
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