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SMR LATERALIZED CONNECTOR 1374.15.314Recalls & reported problems

Limacorporate SPA · Connector Lat +4 mm + Screw - SMALL-R · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390152112), received between Jan 29, 2026 and Jan 29, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Unstable1

Patient problems

  • Joint Laxity1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 29, 2026Unstable

    ON (B)(6) 2019, PATIENT HAD LEFT REVERSE TOTAL SHOULDER. ON (B)(6) 2020, PATIENT DISLOCATED SHOULDER FOR THE FIRST TIME. WHEN VISITING THE LOCAL URGENT CARE, THE SHOULDER COULD NOT BE REDUCED. PATIENT FELL ASLEEP AND SOMEHOW HIS SHOULDER REDUCED. X-RAY REVEALS A WELL REDUCED REVERSE TSA, NO FX'S. THE DOCTOR NOTES: "IF HE DISLOCATES AGAIN, WE WILL HAVE TO CONSIDER A CONSTRAINED LINER WITH OR WITHOUT AN EXTENSION." ON (B)(6) 2020, VISIT THE DOCTOR NOTES "HE APPEARS TO HAVE TORN HIS SUBSCAPULARIS", WHICH HE STATES, "THERE IS NO REASON TO GO BACK AND DO ANYTHING". DURING ON (B)(6) 2022 VISIT, THE DOCTOR NOTED THE FOLLOWING: "HE HAS HAD 2 ADDITIONAL EPISODES OF SUBLUXATION/DISLOCATION. THE MOST RECENT WAS ON (B)(6) 2021, WHICH HE WAS ABLE TO REDUCE ON HIS OWN." TREATMENT OPTIONS WERE DISCUSSED, AND THE DOCTOR REQUESTED A CUSTOM-MADE DEVICE 44MM ALL POLY GLENOSPHERE. DOCTOR ALSO MENTIONS "POSSIBILITY OF AN INFECTION". CULTURES WERE SENT BUT THE MANUFACTURED DID NOT RECEIVE THE OUTCOME. THE COMPONENTS INVOLVED IN THIS EVENT ARE THE FOLLOWING: SMR SMALL-R CONNECTOR +4 (PART CODE: 1374.15.314, LOT NUMBER: 1915239, STERILIZATION: 1900342) SMR METAL-BACK GLENOID SMALL R (PART CODE: 1375.21.00

    Patient problems: Joint Laxity

    MAUDE report 24207499 ↗

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Sources and updates

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