Reported Feb 4, 2026 · Ongoing
AlternatiV+ Max Knotless Anchor
Aju Pharm Co., Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aju Pharm Co., Ltd. · Room 201, Room 207, Bl A · Seongnam, N/A · N/A
Is this the product you have?
- AlternatiV+ Max Knotless Anchor
- Lot codes and dates
- Model No. 20KPN4751, 20KPN5501; All UDI Codes; All Lots.
- Amount recalled
- 2,569 units
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
This product could cause temporary or reversible health problems — stop using it.
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