Arthrex® AR-9107-02-15RRecalls & reported problems
Arthrex, Inc. · AUGMENTED VAULTLOCK, MEDIUM 15R · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867350700), received between Nov 6, 2024 and Mar 18, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fitting 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fitting Problem1
- Material Twisted/Bent1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 18, 2026Material Twisted/Bent
ON (B)(6) 2026, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT AR-9107-02-15R UNIVERS VAULTLOCK AUGMENTED GLENOID PEGS BENT AS IT WAS BEING IMPACTED. THIS ISSUE WAS DISCOVERED DURING A PROCEDURE ON (B)(6) 2026. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Insufficient Information
MAUDE report 24625601 ↗MalfunctionNov 6, 2024Fitting Problem; Fitting Problem
ON 10/24/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT AN AR-9107-02-15R UNIVERS VAULTLOCK AUGMENTED GLENOID WOULD NOT BE INSERTED EVEN AFTER CONFIRMATION VIA PROPER GLENOID PREP AND TRAILING. THE CASE WAS COMPLETED USING A NEW UNIVERS VAULTLOCK AUGMENTED GLENOID. THIS WAS DISCOVERED DURING A PROCEDURE ON (B)(6) 2024.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20623653 ↗
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- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 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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