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Limacorporate S.p.A recalls SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
Recalled April 5, 2023 · FDA recall Z-1317-2023 · Limacorporate S.p.A
Hazard
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. · FDA Class II
Units
1
Sold at
US: MO
Description
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.
Product
SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
Manufacturer(s)
Limacorporate S.p.A
Made in
Italy
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →