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Medium risk Medical DevicesClass II

AlternatiV+ Screw-In Anchor Recall

AlternatiV+ Screw-In Anchor

Updated December 17, 2025

Aju Pharm's AlternatiV+ Screw-In Anchor surgical implant has been recalled due to reports of device failure, including breakage, bending, pull-out, and suture failure. These failures could compromise the surgical repair it was designed to support.

Is the Aju Pharm Co., Ltd. recalled? Yes. This product was recalled by FDA on December 17, 2025. Details below.

What is recalled

AlternatiV+ Screw-In Anchor, manufactured by Aju Pharm Co., Ltd.

Am I affected

You're affected if you have had this surgical implant placed or if you received a package of these anchors for medical use. Check with your surgeon or healthcare provider if you're unsure whether your repair used this device.

What to do right now

Contact your surgeon or healthcare provider immediately to discuss whether you received this implant and whether any follow-up examination or replacement is needed.

The hazard

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

Brands affected

Aju Pharm Co., Ltd.
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1173-2026
Classification
Class II
Recalled
December 17, 2025
Read the official notice

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