Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by Arthrosurface, Inc. Due to Fully threaded Taper Post Fixation components not cleared...
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 Arthrosurface, Inc. directly.
Affected Products
Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
Quantity: 182 units
Why Was This Recalled?
Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Arthrosurface, Inc.
Arthrosurface, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report