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Medium severity

AlternatiV+ Max Knotless Anchor

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateDecember 17, 2025
ReportedFebruary 04, 2026
Recalling firmAju Pharm Co., Ltd.
Country / regionKorea (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

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