Device recall
Z-0884-04: STS-T Mobile x-ray system used with the STS-T lithotripter.
FDA device recall · Class II · Medstone International Inc
Key facts
| Recall number (Z-number) | Z-0884-04 |
|---|---|
| Recall event | 29909 |
| Product | STS-T Mobile x-ray system used with the STS-T lithotripter. |
| Recalling firm | Medstone International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 1, 2004 |
| PMA numbers | P870015 |
| FEI number | 2082981 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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