AlternatiV+ Max Knotless Anchor recall
AlternatiV+ Max Knotless Anchor
Why was AlternatiV+ Max Knotless Anchor recalled?
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model No. 20KPN4751, 20KPN5501; All UDI Codes; All Lots.
- Product
- AlternatiV+ Max Knotless Anchor
- Recalling firm
- Aju Pharm Co., Ltd.
- Quantity
- 2,569 units
- Distribution
- US Nationwide distribution in the states of CA & PR.
- Recall date
- February 4, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)