Arthrex® AR-9501-11CPCRecalls & reported problems
Arthrex, Inc. · UNIVERS REVERS STEM, SIZE 11, CAP COATED · 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 00888867061064), received between Jan 5, 2026 and Jan 5, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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
- Patient Device Interaction Problem1
Patient problems
- Bone Fracture(s)1
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 5, 2026Patient Device Interaction Problem
IT WAS REPORTED THAT THE INVERS SHOULDER PROTHESIS WAS INITIALLY IMPLANTED ON (B)(6) 2020. A CRASH ON (B)(6) 2020, CAUSED A PERIPROSTHETIC FRACTURE, WHICH WAS TREATED CONSERVATIVELY. THE FRACTURE SUBSEQUENTLY HEALED. THE LAST IMAGES TAKEN ON (B)(6) 2022, SHOWED THAT THE IMPLANT WAS IN THE CORRECT POSITION. THE X-RAYS TAKEN ON (B)(6) 2025, SHOWED A FRACTURE BETWEEN THE CUP AND THE SHAFT. THE IMPLANT WAS REMOVED ON (B)(6) 2025.
Patient problems: Bone Fracture(s); Insufficient Information
MAUDE report 23956323 ↗
Other Shoulder Prosthesis, Reverse Configuration devices
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- 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.
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