Device recall
Z-1615-2020: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1615-2020 |
|---|---|
| Recall event | 85143 |
| Product | Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for primary, fracture, or revision total shoulder replacement for the relief of pain and significant disability due to gross rotator cuff deficiency Item Number: 010000589 |
| Product code | PHX |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 5, 2020 |
| 510(k) numbers | K120121 |
| 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