Device recall
Z-1867-2017: 216 Wilson Frame Pads, Model # 5319-37; Used with Radiolucent Wilson Frames…
FDA device recall · Class II · Mizuho OSI
Key facts
| Recall number (Z-number) | Z-1867-2017 |
|---|---|
| Recall event | 76920 |
| Product | 216 Wilson Frame Pads, Model # 5319-37; Used with Radiolucent Wilson Frames, model numbers 5319G and 5321G. General and Plastic Surgery: These pads are used as a component of the Wilson Frames, which support the torso of a prone patient during spine surgery. The pads are supplied with the frames and… |
| Product code | FWZ |
| Recalling firm | Mizuho OSI |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2017 |
| 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