Device recall
Z-0424-03: X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller…
FDA device recall · Class II · X-Cel X-Ray Corp
Key facts
| Recall number (Z-number) | Z-0424-03 |
|---|---|
| Recall event | 25571 |
| Product | X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012 |
| Product code | KPR-- |
| Recalling firm | X-Cel X-Ray Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 28, 2003 |
| FEI number | 1418484 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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