Arthrex® AR-8916CX24-18Recalls & reported problems
Arthrex, Inc. · LOW PROFILE SCREW, 2.4MM X 18MM CORTEX · 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 00888867219724), received between May 8, 2024 and May 8, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (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
- Unintended Movement1
Patient problems
- 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.
MalfunctionMay 8, 2024Unintended Movement; Unintended Movement
IT WAS REPORTED THAT DURING A PROCEDURE THE SURGEON HAD AN ISSUE WITH A VOLAR DISTAL RADIUS PLATE. THE DISTAL 2.4 LOCKING SCREWS WOULD NOT LOCK INTO THE PLATE AND JUST SPUN IN PLACE. THE SURGEON THEN TOOK OUT THE PLATE, REPLACED WITH ANOTHER PLATE AND DID NOT WANT TO USE ANY OF THE SCREWS FROM THIS SET. NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19271102 ↗
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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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