PlainRecalls
FDA Devices Moderate Class II Ongoing

Genesis Knotless Anchor

Reported: February 4, 2026 Initiated: December 17, 2025 #Z-1170-2026

Product Description

Genesis Knotless Anchor

Reason for Recall

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

Details

Recalling Firm
Aju Pharm Co., Ltd.
Units Affected
1,163 units
Distribution
US Nationwide distribution in the states of CA & PR.
Location
Seongnam, N/A

Frequently Asked Questions

What product was recalled?
Genesis Knotless Anchor. Recalled by Aju Pharm Co., Ltd.. Units affected: 1,163 units.
Why was this product recalled?
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 4, 2026. Severity: Moderate. Recall number: Z-1170-2026.