Device recall
Z-0518-2024: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix…
FDA device recall · Class II · Riverpoint Medical, LLC
Key facts
| Recall number (Z-number) | Z-0518-2024 |
|---|---|
| Recall event | 93390 |
| Product | Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 3911-714-521 The Iconix Knotless anchors are intended to be used for soft-tissue to bone fixation in the foot, ankle, knee, hip, hand, wrist, elbow and shoulder. |
| Product code | MBI |
| Recalling firm | Riverpoint Medical, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K231278 |
| FEI number | 3006981798 |
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