Aju Pharm Co., Ltd. Recall
AlternatiV+ Screw-In Anchor
Updated December 17, 2025
Aju Pharm Co., Ltd. is recalling AlternatiV+ Screw-In Anchor. Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
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
Am I affected
You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.
What to do right now
Voluntary: Firm initiated
The hazard
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-Z-1173-2026
- Classification
- Class II
- Recalled
- December 17, 2025
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