Limacorporate S.p.A: Medical Device Recall in 2023 - (Recall #: Z-1317-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210

Product Classification:

Class II

Date Initiated: February 21, 2023

Date Posted: April 5, 2023

Recall Number: Z-1317-2023

Event ID: 91869

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 1

Code Information:

UDI-DI/Lot/Expiration: 08033390121798/2206565/2027-04-30

Distribution Pattern:

US: MO

Voluntary or Mandated:

Voluntary: Firm initiated