Device recall
Z-0924-2011: Mizuho ProFx 6850 Operating Room Table, with orthopedic accessories, AC Powered…
FDA device recall · Class II · Mizuho Orthopedic Systems Inc
Key facts
| Recall number (Z-number) | Z-0924-2011 |
|---|---|
| Recall event | 56859 |
| Product | Mizuho ProFx 6850 Operating Room Table, with orthopedic accessories, AC Powered, manufactured by Mizuho OSI, Union City, CA. |
| Product code | JEA |
| Recalling firm | Mizuho Orthopedic Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2011 |
| FEI number | 2921578 |
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