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
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 ↗
Other Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented devices
- DJO SURGICAL 508-32-204Encore Medical, L.P. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall544 reports
- Comprehensive Reverse Shoulder 010000589Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- DELTA XTEND 130738203Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DJO SURGICAL 509-00-432Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 recall117 reports
- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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