Device recall
Z-0780-2007: Doro Products Adapter, Product number 5979-300. The adaptor system is attached…
FDA device recall · Class II · Orthopedic Systems Inc
Key facts
| Recall number (Z-number) | Z-0780-2007 |
|---|---|
| Recall event | 37510 |
| Product | Doro Products Adapter, Product number 5979-300. The adaptor system is attached to OSI''s Spinal Frame, which is an operating room tabletop that is attached to a table base. The Frame is used to support patients during spinal surgery. |
| Product code | FWZ |
| Recalling firm | Orthopedic Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 6, 2007 |
| 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