Device recall
Z-0093-2021: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0093-2021 |
|---|---|
| Recall event | 86422 |
| Product | Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis item: 010000589 - Product Usage: intended to serve as the foundation for the reverse shoulder prosthesis head (glenosphere). |
| Product code | PHX |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 31, 2020 |
| 510(k) numbers | K120121, K193373 |
| 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