Device recall
Z-0789-2007: AMS 700 LGX MS Pump IZ Preconnected penile Prosthesis with InhibiZone, product…
FDA device recall · Class II · American Medical Systems
Key facts
| Recall number (Z-number) | Z-0789-2007 |
|---|---|
| Recall event | 37437 |
| Product | AMS 700 LGX MS Pump IZ Preconnected penile Prosthesis with InhibiZone, product length 15 cm, product number 72404251. Penoscrotal Approach - with InhibiZone, 1 MS Pump, 2 Cylinders. |
| Product code | JCW |
| Recalling firm | American Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2008 |
| FEI number | 1000116179 |
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