LATERALIZED AND AUGMENTED BASEPLATE 105-0029Recalls & reported problems
Fx Solutions · TA6V CEMENTLESS GLENOID BASEPLATE W/ SCREW Ti/HA Ø24mm, +3mm LATERALIZED · Class 2 · Implant
Data updated Oct 16, 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 03701037316801), received between Jul 9, 2026 and Jul 9, 2026 — classified as 1 injury.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Migration1
Patient problems
- Inadequate Osseointegration1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 9, 2026Migration
REVISION OCCURRED ON (B)(6) 2026 APPROXIMATELY 56 DAYS AFTER THE PRIMARY WHICH OCCURRED ON (B)(6) 2026. NO FALL OR OTHER TRAUMA WAS REPORTED. BASED ON COMPARING USAGE FORMS HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEPLATE W/ SCREW TI/HA Ø24MM, +3MM LATERALIZED AND HUMELOCK REVERSED CENTERED GLENOSPHERE W/ SCREW COCR/TA6V/TIN 10° TILT Ø32MM WAS EXPLANTED DUE TO LOOSENING AND REPLACED WITH POST EXTENSION TA6V +10MM CEMENTLESS TI/HA, LOCKING SCREW TA6V Ø4.5MM L.30MM, FX V135 HUMERAL CUP 135/145° STANDARD PE/TA6V Ø40 +3, HUMELOCK REVERSED CENTERED GLENOSPHERE W/SCREW COCR/TA6V/TIN 10° TILT Ø40MM, LOCKING SCREW TA6V Ø4.5MM L.20MM, LOCKING SCREW TA6V Ø4.5MM L.25MM, HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEPLATE TI/HA Ø24MM AND LOCKING SCREW TA6V Ø4.5MM L.30MM. FX V135® HUMELOCK STEM TA6V Ø32/10 L. 120MM CEMENTLESS TI/HA WAS NOT REPLACED.
Patient problems: Inadequate Osseointegration
MAUDE report 25765664 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page