AlternatiV+ Max Knotless Anchor
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | December 17, 2025 |
| Reported | February 04, 2026 |
| Recalling firm | Aju Pharm Co., Ltd. |
| Country / region | Korea (the Republic of) N/A |
Hazard
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Affected products
- AlternatiV+ Max Knotless Anchor
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