Device recall
Z-1833-2015: PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND…
FDA device recall · Class II · ArthroCare Medical Corporation
Key facts
| Recall number (Z-number) | Z-1833-2015 |
|---|---|
| Recall event | 71311 |
| Product | PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck, oral, and sinus surgery… |
| Product code | GEI |
| Recalling firm | ArthroCare Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2016 |
| 510(k) numbers | K142999 |
| 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