Device recall
Z-1658-2008: Biomet Hybrid Glenoid Boss Cutter; item 406150. - Surgical instrument used to…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1658-2008 |
|---|---|
| Recall event | 47238 |
| Product | Biomet Hybrid Glenoid Boss Cutter; item 406150. - Surgical instrument used to prepare the natural shoulder glenoid surface for implanting a Hybrid Glenoid component. This instrument is intended to function by drilling a hole into the natural glenoid surface allowing the center boss of glenoid… |
| Product code | KWT |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 15, 2008 |
| 510(k) numbers | K060694 |
| FEI number | 1825034 |
At a glance
- 1–9 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