FDADecember 17, 2025device
Fixone Hybrid Anchor
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
What to do
FDA enforcement status: Ongoing
Brands named
aju pharmaju
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAGenesis Knotless Anchor2025-12-17
- FDAAlternatiV+ Screw-In Anchor2025-12-17
- FDAGenesis Screw-In Anchor2025-12-17
- FDAGenesis Dual Thread Screw-In Anchor2025-12-17
- FDAGenesis Push-In Suture Anchor2025-12-17
- FDAAlternatiV+ Max Knotless Anchor2025-12-17
- FDAFixone Biocomposite Anchor2025-12-17
- FDANandrolone Decanoate 200 mg/mL Injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-68462019-05-23
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