Humelock Reversed Shoulder 313-4010Recalls & reported problems
Fx Solutions · HUMELOCK REVERSED STEM TA6V CEMENTED Ø40/10 · Class 2 · Implant
All models of Humelock Reversed Shoulder (13)
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 03701037301449), received between May 27, 2021 and May 27, 2021 — classified as 1 injury.
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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Device Dislodged or Dislocated1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 27, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
THE EVENT WAS A REVISION SURGERY DUE TO DISLOCATION APPROXIMATELY 1 MONTH AFTER THE PRIMARY SURGERY. THE PRIMAR SURGERY USED THE HUMELOCK REVERSED SYSTEM. DURING HE REVISION SURGERY, THE SURGEON EXPLANTED THE SIZE 10 CEMENTED STEM, THE +9MM HUMERAL SPACER AND THE Ø36/+6 STANDARD HUMERAL CUP. THEN HE IMPLANTED A SIZE 12 CEMENTLESS STEM, A Ø36/+9 STANDARD HUMERAL CUP AND A NEW +9MM HUMERAL SPACER. CLINICAL CASE OF RETROSPECTIVE STUDY.
Patient problems: Insufficient Information
MAUDE report 11892147 ↗
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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