Device recall
Z-1203-2012: Coupler System II Mizuho Orthopedic Systems, Inc. Union City, CA 94587 The 5873…
FDA device recall · Class II · Mizuho Orthopedic Systems Inc
Key facts
| Recall number (Z-number) | Z-1203-2012 |
|---|---|
| Recall event | 61275 |
| Product | Coupler System II Mizuho Orthopedic Systems, Inc. Union City, CA 94587 The 5873 Coupler II is designed for use specifically with the Mizuho OSI Modular Base and the Spinal System Table Tops (AKA Jackson Spinal Table Top). The Coupler II mounts onto the Spinal Surgery Top by using the Spinal Top… |
| Product code | FWZ |
| Recalling firm | Mizuho Orthopedic Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2012 |
| 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