Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SYSTEM 26. Part Numbers: OS900035-NS Recalled by ORTHO SOLUTIONS, LTD. Due to Following the identification of corrosion residue found inside...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ORTHO SOLUTIONS, LTD. directly.
Affected Products
SYSTEM 26. Part Numbers: OS900035-NS; OS900036-NS; OS900037-NS; OS900038-NS; OS900040-NS; OS900041-NS; OS900042-NS; OS900043-NS; OS900047-NS; OS900048-NS; OS900045-NS; OS900046-NS; OS900050-NS; OS900051-NS; OS900044-NS; OS900049-NS; OS900053-NS; OS900054-NS; OS900055-NS; OS900056-NS; OS900058-NS; OS900059-NS; OS900057-NS.
Quantity: 120
Why Was This Recalled?
Following the identification of corrosion residue found inside the cannulated devices in Forefoot and Midfoot trays Orhto Solutions Group has taken the decision to recall ALL x106 System 26 Forefoot and Midfoot Implants and Instruments tray from the US market.
Where Was This Sold?
U.S.
About ORTHO SOLUTIONS, LTD.
ORTHO SOLUTIONS, LTD. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report