Device recall
Z-2987-2026: Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas…
FDA device recall · Class II · restor3d Inc.
Key facts
| Recall number (Z-number) | Z-2987-2026 |
|---|---|
| Recall event | 99402 |
| Product | Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030; 1500-1035 Software Version: N/A - off-the-shelf hardware product Product Description: The restor3d Reverse Total Shoulder Arthroplasty System is intended for patients… |
| Product code | PHX |
| Recalling firm | restor3d Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K243643 |
| FEI number | 3014833750 |
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