Arthrex® AR-9551-06Recalls & reported problems
Arthrex, Inc. · UNIVERS REVERS TRIAL SPACER 36+6MM · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867062351), received between Feb 13, 2023 and Feb 13, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 13, 2023Break
IT WAS REPORTED ON (B)(6) 2023 BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-9551-06 TRIAL SPACER BROKE DURING TRIAL. CASE INVOLVEMENT, DEVICE BROKE DURING USE. PER FACILITY: " THE INSTRUMENT WAS BROKEN IN TWO PARTS AND BOTH PIECES WERE SUCCESSFULLY REMOVED. THERE WAS NO UNPLANNED INCISION AND REMOVAL OF THE BROKEN PIECE TOOK AN ADDITIONAL 10 SECONDS. A SECOND SURGERY IS NOT NECESSARY."
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16361562 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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