Arthrex® AR-611-10Recalls & reported problems
Arthrex, Inc. · iBalance UKA, Tibia Peg Drill · Class 1
Data updated Oct 16, 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 00888867223899), received between Jul 28, 2023 and Jul 28, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Fragmentation” (2 reports).
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.
Most reported problems
Device problems
- Material Fragmentation2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 28, 2023Material Fragmentation; Material Fragmentation
ON 06/21/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-611-10 TIBIA PEG DRILL AND AR-611-11 FEMORAL PEG DRILL ARE WORN AND PIECES ARE STARTING TO SHAVE OFF. THIS WAS DISCOVERED DURING A CASE AND PRODUCED DEBRIS.
Patient problems: Insufficient Information
MAUDE report 17413900 ↗MalfunctionJul 28, 2023Material Fragmentation; Material Fragmentation
ON 06/21/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-611-10 TIBIA PEG DRILL AND AR-611-11 FEMORAL PEG DRILL ARE WORN AND PIECES ARE STARTING TO SHAVE OFF. THIS WAS DISCOVERED DURING A CASE AND PRODUCED DEBRIS.
Patient problems: Insufficient Information
MAUDE report 17413878 ↗
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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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