Device recall
Z-0243-2008: OSI, 6822 IntraOp Series Tables, Operating Room tables, Orthopedic Systems…
FDA device recall · Class II · Mizuho Orthopedic Systems Inc
Key facts
| Recall number (Z-number) | Z-0243-2008 |
|---|---|
| Recall event | 38307 |
| Product | OSI, 6822 IntraOp Series Tables, Operating Room tables, Orthopedic Systems, Inc., Union City, CA. (Series 6800 and 6822 included) |
| Product code | LHN |
| Recalling firm | Mizuho Orthopedic Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 18, 2008 |
| 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