Device recall
Z-0704-03: Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers.
FDA device recall · Class II · Midmark Corp
Key facts
| Recall number (Z-number) | Z-0704-03 |
|---|---|
| Recall event | 25727 |
| Product | Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers. |
| Product code | FLE |
| Recalling firm | Midmark Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2004 |
| FEI number | 1523530 |
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