Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210
Brand
Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy
Lot Codes / Batch Numbers
UDI-DI/Lot/Expiration: 08033390121798/2206565/2027-04-30
Products Sold
UDI-DI/Lot/Expiration: 08033390121798/2206565/2027-04-30
Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy is recalling SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210 due to Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On 2/21/23, a recall notice was distributed to a customer who was asked to do the following: 1) Check your stock to locate and quarantine the affected devices. Devices must be sent back. 2) Complete, and return the response form to pms@limacorporate.com 3) The recall notice should be shared with anyone who needs to be aware within your organization or shared with any organization where the potentially affected products have been transferred. Inquiries can be sent to medicalcomplaints@limacorporate.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
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Page updated: Jan 10, 2026