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Aju Pharm Co., Ltd. recalls AlternatiV+ Max Knotless Anchor
Recalled February 4, 2026 · FDA recall Z-1172-2026 · Aju Pharm
Hazard
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. · FDA Class II
Units
2,569 units
Sold at
US Nationwide distribution in the states of CA & PR.
Description
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Product
AlternatiV+ Max Knotless Anchor
Manufacturer(s)
Aju Pharm Co., Ltd.
Made in
Korea (the Republic of)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →