Device recall
Z-0621-2021: Custom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0621-2021 |
|---|---|
| Recall event | 86896 |
| Product | Custom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1. Noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis 3. Correction of functional deformity 4. Treatment of non-union, femoral neck fracture, and trochanteric… |
| Product code | LPH |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2024 |
| 510(k) numbers | K991807 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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