Seongnam, N/A, Korea (the Republic of)
Aju Pharm Co., Ltd. recalls
1 recall recorded since 2018, most recently on 17 December 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 17 December 2025
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1173-2026, Z-1171-2026, Z-1167-2026, Z-1166-2026, Z-1170-2026, Z-1172-2026, Z-1169-2026, Z-1168-2026
- AlternatiV+ Screw-In Anchor
- Genesis Push-In Suture Anchor
- Fixone Biocomposite Anchor
- Fixone Hybrid Anchor
- Genesis Knotless Anchor
- AlternatiV+ Max Knotless Anchor
- Genesis Dual Thread Screw-In Anchor
- Genesis Screw-In Anchor
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.