Device recall
Z-0888-06: XLie with Tubing, 12 cm, Electrosurgical Device-RITA * Medical Systems, Inc. *…
FDA device recall · Class II · Rita Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0888-06 |
|---|---|
| Recall event | 35342 |
| Product | XLie with Tubing, 12 cm, Electrosurgical Device-RITA * Medical Systems, Inc. * StarBurst Xli enhanced with tubing set * * REF/Catalog: 700-103027 * 4-7 cm Diameter * 12cm Length * Sterile/R * RITA * Manufactured by: Rita Medical Systems, Inc., One Horizon Way, Manchester, Georgia 31816, USA |
| Product code | GEI |
| Recalling firm | Rita Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2008 |
| 510(k) numbers | K010060 |
| FEI number | 3017892510 |
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