Device recall
Z-1674-2023: LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz…
FDA device recall · Class II · Linkbio Corp.
Key facts
| Recall number (Z-number) | Z-1674-2023 |
|---|---|
| Recall event | 92294 |
| Product | LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision total knee replacement. Item Number: 880-325/13 |
| Product code | JWH |
| Recalling firm | Linkbio Corp. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K202924 |
| FEI number | 3006721341 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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