Arthrex® AR-8724V-30Recalls & reported problems
Arthrex, Inc. · 2.4 X 30MM VAL SCREW, Ti · Class 2 · Implant
Data updated Oct 18, 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 00888867045675), received between Sep 14, 2017 and Sep 14, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Malposition of Device” (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
- Malposition of Device1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 14, 2017Malposition of Device
IT WAS ORIGINALLY REPORTED THAT THE SCREWS BEGAN TO CHANGE ANGLE AFTER BEING IMPLANTED. FOLLOW-UP INVESTIGATION: IT WAS REPORTED THAT THE PATIENT UNDERWENT DISTAL RADIUS REPAIR ON (B)(6) 2017. ON (B)(6) 2017 THE PATIENT WAS EXPERIENCING PAIN AND DISPLACEMENT. THE VOLAR DISTAL RADIUS PLATE ALONG WITH ALL THE SCREWS WERE REMOVED ON (B)(6) 2017. THE ISSUE WAS FOUND DURING ROUTINE FOLLOW UP WITH X-RAYS. NO ARTHREX DEVICES WERE IMPLANTED DURING REVISION SURGERY.
Patient problems: Pain
MAUDE report 6864205 ↗
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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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