Arthrex® AR-8973L-30-180Recalls & reported problems
Arthrex, Inc. · 3.0X180MM FIBULA NAIL, LEFT · Class 2 · Implant
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 00888867295223), received between Apr 30, 2024 and Apr 30, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective 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.
Reports received per month
Most reported problems
Device problems
- Defective Device1
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.
MalfunctionApr 30, 2024Defective Device; Defective Device
ON 11/15/2021, IT WAS REPORTED BY A FACILITY REPRESENTATIVE VIA E-MAIL THAT A AR-8973L-30-180 FIBULOCK NAIL INNER PACKAGING MAY BE RUSTED. THIS WAS DISCOVERED DURING A CASE WHEN ONE OF THE SALES REPRESENTATIVES OPENED THE BOX TO THE FIBULOCK NAIL AND IT WAS FOUND TO HAVE SOME SORT OF SUBSTANCE OR RUST INSIDE. THERE WAS NO PATIENT EFFECT REPORTED.
Patient problems: Insufficient Information
MAUDE report 19214633 ↗
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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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