Class II

Medical Device Recall: AlternatiV+ Max Knotless Anchor

Aju Pharm Co., Ltd. · December 17, 2025

Reason for Recall

Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.

Distribution

US Nationwide distribution in the states of CA & PR.

States Affected

NATIONWIDE

Quantity Affected

2,569 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1172-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.