Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SMR TT Hybrid glenoid Std - Peg S Recalled by Limacorporate S.p.A Due to Shoulder glenoid fossa prosthesis was manufactured without tantalum...
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 Limacorporate S.p.A directly.
Affected Products
SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
Quantity: 1
Why Was This Recalled?
Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct radiographic assessment of the hybrid glenoid position can be performed by the evaluation of the joint space, central TT peg position and cement mantel observation.
Where Was This Sold?
This product was distributed to 1 state: MO
About Limacorporate S.p.A
Limacorporate S.p.A has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report