Glenoid Baseplate with Screw 105-0028Recalls & reported problems
Fx Solutions · HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEPLATE W/ SCREW Ti/HA Ø24mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03701037313305), received between Apr 25, 2022 and Oct 18, 2024 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
- Migration1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Joint Dislocation1
- Joint Laxity1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 18, 2024Migration; Migration
THE PATIENT WAS REVISED DUE TO LOOSENING ON (B)(6) 2024. THE IMPLANTATION DATE WAS ON (B)(6) 2023.A GLENOSPHERE, A METAGLENE AND SCREWS WERE EXPLANTED. AN HELMET HEAD AND DOUBLE TAPER WERE IMPLANTED.
Patient problems: Joint Laxity
MAUDE report 20479039 ↗InjuryFeb 27, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION OCCURRED ON (B)(6) 2024, APPROXIMATELY 2 WEEKS AFTER THE PRIOR REVISION ON (B)(6) 2024. PRIMARY SURGERY OCCURRED ON (B)(6) 2023. NO FALL OR OTHER TRAUMA REPORTED. REVISION OCCURRED DUE TO DISLOCATION OF UNKNOWN CAUSE. THE FIRST REVISION OCCURRED FOR A SIMILARLY AMBIGUOUS REASON. THIS SECOND REVISION WAS A REPLACEMENT OF EVERYTHING EXCEPT THE STEM. EXPLANT OF 24 MM BASEPLATE, 32 MM CENTERED GLENOSPHERE, 32 MM + 3 STABILITY HUMERAL CUP, 9 MM SPACER, AND 5 SCREWS. IMPLANT OF 24 MM BASEPLATE, 36 MM ECCENTRIC GLENOSPHERE, 36 MM + 3 STABILITY HUMERAL CUP, 9 MM SPACER, AND 4 SCREWS.
Patient problems: Joint Dislocation
MAUDE report 18793393 ↗InjuryApr 25, 2022Device Dislodged or Dislocated
THE PATIENT WAS REVISED ON (B)(6) 2022 FOLLOWING THE INITIAL SURGERY ON (B)(6) 2022 DUE TO DISLOCATION. THE SURGEON EXPLANTED GLENOID BASEPLATE (24), CENTERED GLENOSPHERE (40), HUMERAL CUP (40/9), STANDARD SCREW (40MM) AND 2 LOCKING SCREWS (20MM AND 40 MM EACH). THE SURGEON IMPLANTED GLENOID BASEPLATE (24), CENTERED GLENOSPHERE (40), HUMERAL CUP (40/6), A CENTRAL SCREW (14MM), 2 STANDARD SCREWS (20MM AND 35 MM EACH) AND 2 LOCKING SCREWS (30MM AND 40 MM EACH).
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 14197049 ↗
Other Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented devices
- DJO SURGICAL 509-02-032Encore Medical, L.P. · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED364 reports
- DELTA XTEND 130790036Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED171 reports
- DELTA XTEND 130770018Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED159 reports
- TRIGEN 71118200Smith & Nephew, Inc. · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED123 reports
- DJO SURGICAL 509-02-432Encore Medical, L.P. · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED119 reports
- DELTA XTEND 130738206Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED116 reports
- COMPREHENSIVE SHOULDER SYSTEM 113633Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED2 recalls4 reports
- DELTA XTEND 130742206Depuy (Ireland) · PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED99 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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