Device recall
Z-1113-2015: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number…
FDA device recall · Class II · Arthrosurface, Inc.
Key facts
| Recall number (Z-number) | Z-1113-2015 |
|---|---|
| Recall event | 69723 |
| Product | Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component. |
| Product code | HSD |
| Recalling firm | Arthrosurface, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2015 |
| 510(k) numbers | K023096 |
| FEI number | 3004154314 |
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