Class IIReported 2026-02-04

Genesis Knotless Anchor

Recalled by Aju Pharm Co., Ltd.

Reason for Recall

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

Recall Number

Z-1170-2026

Classification

Class II

Status

Ongoing

Category

device

Initiated

2025-12-17

Reported

2026-02-04

Distribution

US Nationwide distribution in the states of CA & PR.

Code Info

Model No. 10KPN4751, 10KPN5501; All UDI Codes; All Lots.

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.