Arthrex® AR-8963AL-12Recalls & reported problems
Arthrex, Inc. · ANTEROLAT DIST TIB PLT, SS, LEFT, 12H · Class 2 · Implant
Data updated Oct 16, 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 00888867223097), received between Jan 27, 2020 and Jan 27, 2020 — classified as 1 injury.
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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 27, 2020Break
IT WAS REPORTED THAT THE IMPLANTED PLATE BROKE FOUR WEEKS AFTER THE INITIAL SURGERY. A REVISION SURGERY WAS PERFORMED ON (B)(6) 2019. THE SURGEON HAS USED A NAIL TO SUCCESSFULLY PERFORM THE SURGERY. ADDITIONAL INFORMATION 14-JAN-2020: FURTHER INFORMATION WERE RECEIVED THAT THE INITIAL PROCEDURE WAS A REVISION TIBIA & FIBULA FRACTURE SURGERY.
Patient problems: No Code Available
MAUDE report 9631820 ↗
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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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