Device recall
Z-1073-2007: Gyrus CyberWand Ultrasonic Lithotripter System includes: CW-USLS CyberWand USL…
FDA device recall · Class II · Gyrus ACMI Corporation
Key facts
| Recall number (Z-number) | Z-1073-2007 |
|---|---|
| Recall event | 37999 |
| Product | Gyrus CyberWand Ultrasonic Lithotripter System includes: CW-USLS CyberWand USL System CW-USLT CyberWand USL Transducer CW-USLRBP CyberWand USL Renal/Bladder Probe Set CW-USLTT CyberWand USL Transducer Sterilization Tray |
| Product code | FFK |
| Recalling firm | Gyrus ACMI Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 25, 2010 |
| 510(k) numbers | K052135 |
| FEI number | 3003790304 |
At a glance
- 1–9 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