Aju Pharm Recalls
8 recalls on record · February 4, 2026 to February 4, 2026 · Medical Devices
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls AlternatiV+ Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls AlternatiV+ Max Knotless Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Push-In Suture Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Knotless Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Dual Thread Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Fixone Biocomposite Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Fixone Hybrid Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.