Arthrex® AR-1407LP-50Recalls & reported problems
Arthrex, Inc. · REAMER, LOW PROFILE · 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 00888867016699), received between May 10, 2021 and May 10, 2021 — 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
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 10, 2021Break
IT WAS REPORTED THAT THE REAMER BROKE UPON COMING IN CONTACT WITH THE BONE WHILE THE SURGEON WAS ATTEMPTING TO DRILL A TIBIAL TUNNEL. ONE WING OF THE BROKEN REAMER WAS LOCATED AND THE OTHER WAS NOT. AN X-RAY WAS USED TO SCAN THE PATIENT'S LEG AND NO METAL FRAGMENTS WERE LOCATED.
Patient problems: Insufficient Information
MAUDE report 11800855 ↗
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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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