Device recall
Z-2227-2017: Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used…
FDA device recall · Class II · Orthosoft, Inc. dba Zimmer CAS
Key facts
| Recall number (Z-number) | Z-2227-2017 |
|---|---|
| Recall event | 75609 |
| Product | Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the tracking software as part of the software based navigation systems. The affected Sesamoid Plasty components are the central structural column and its base that hold up the computer and the tracking camera on… |
| Product code | HAW |
| Recalling firm | Orthosoft, Inc. dba Zimmer CAS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 2, 2017 |
| 510(k) numbers | K071929 |
| FEI number | 3003714383 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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