LATERALIZED AND AUGMENTED BASEPLATE 105-0026Recalls & reported problems
Fx Solutions · TA6V CEMENTLESS GLENOID BASEPLATE W/ PEG Ti/HA Ø24mm, +6mm LATERALIZED · 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 03701037316795), received between May 23, 2025 and Jul 10, 2026 — classified as 3 injuries.
The most frequently reported specific device problem is “Migration” (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 Problem2
- Migration1
Patient problems
- Joint Dislocation2
- Inadequate Osseointegration1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJul 10, 2026Adverse Event Without Identified Device or Use Problem
REVISION OCCURRED ON (B)(6) 2026 APPROXIMATELY 392 DAYS AFTER THE PRIMARY WHICH OCCURRED ON (B)(6) 2025. NO FALL OR OTHER TRAUMA WAS REPORTED. BASED ON COMPARING USAGE FORMS ONLY HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEPLATE W/PEG TI/HA Ø24MM, +6MM LATERALIZED, HUMELOCK REVERSED CENTERED GLENOSPHERE W/ SCREW COCR/TA6V 10° TILT Ø36MM, HUMERAL CUP STANDARD PE/TA6V Ø36/+3, TWO STANDARD SCREW TA6V Ø4.5MM L.30MM AND TWO STANDARD SCREW TA6V Ø4.5MM L.25MM WAS EXPLANTED DUE TO DISLOCATION AND REPLACED WITH OFFSET TAPER ADAPTER TA6V Ø24 / Ø10 AND CENTERED HEAD 50X21. FX V135® HUMELOCK STEM TA6V Ø32/08 L. 120MM CEMENTLESS TI/H WAS NOT REPLACED.
Patient problems: Joint Dislocation
MAUDE report 25781576 ↗InjuryJun 26, 2025Migration; Migration
REVISION OCCURRED APPROXIMATELY 21 MONTHS AFTER THE PRIOR REVISION SURGERY, WHICH OCCURRED ON (B)(6) 2023. THE PRIMARY SURGERY OCCURRED ON (B)(6) 2023. NO FALL OR OTHER TRAUMA REPORTED. REVISION OCCURRED DUE TO LOOSENING OF THE BASEPLATE COMPONENT. A 24 MM + 6 LATERALIZED BASEPLATE, 6 MM POST EXTENSION, 40 MM ECCENTRIC GLENOSPHERE, 40 MM +3 HUMERAL STABILITY CUP, 2 OF 9 MM SPACER, AND 3 STANDARD SCREWS WERE EXPLANTED. THESE ITEMS WERE REPLACED WITH A COMPETITOR ANTIBIOTIC SPACER; FX COMPONENTS WERE LISTED ON THE USAGE FORM FOR THE CASE BUT WERE ALL WASTED.
Patient problems: Inadequate Osseointegration
MAUDE report 22341553 ↗InjuryMay 23, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION OCCURRED APPROXIMATELY 15 WEEKS AFTER THE PRIOR REVISION SURGERY WHICH OCCURRED ON (B)(6) 2025. THE PRIMARY SURGERY OCCURRED ON (B)(6) 2022. NO FALL OR OTHER TRAUMA REPORTED. REVISION OCCURRED DUE TO DISLOCATION OF UNKNOWN CAUSE. 24 MM + 6 LATERALIZED BASEPLATE, 36 MM CENTERED GLENOSPHERE, 36 MM + 9 HUMERAL STABILITY CUP, AND 4 STANDARD SCREWS EXPLANTED. THESE PARTS WERE REPLACED WITH AN IDENTICAL BASEPLATE, A 6 MM POST EXTENSION, 40 MM CENTERED GLENOSPHERE, 40 MM + 9 135/145 STANDARD HUMERAL CUP, 9 MM SPACER, AND 4 STANDARD SCREWS.
Patient problems: Joint Dislocation
MAUDE report 22078356 ↗
Other Shoulder Prosthesis, Reverse Configuration devices
- DJO SURGICAL 508-36-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration508 reports
- DJO SURGICAL 508-32-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration433 reports
- DJO SURGICAL 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 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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