Arthrex® AR-8724V-22SRecalls & reported problems
Arthrex, Inc. · 2.4 X 22MM VAL SCREW, TI, STERILE · Class 2 · Implant
Data updated Oct 16, 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 00888867209817), received between Aug 25, 2025 and Aug 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (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.
Reports received per month
Most reported problems
Device problems
- Difficult or Delayed Positioning1
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.
MalfunctionAug 25, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning
ON 08/07/2025, AN ARTHREX SUBSIDIARY EMPLOYEE REPORTED VIA EMAIL THAT AN AR-8724V-22S LOW PROFILE VA LOCKING SCREW PENETRATED THE AR-8924VSL-03S 2.4 MM VOLAR DISTAL RADIUS PLATE, INCLUDING ITS SCREW HEAD, DURING INSERTION INTO THE BONE HOLE. THE SURGEON REMOVED THE SCREW AND INSERTED A NEW ONE INTO THE SAME BONE HOLE, SUCCESSFULLY ACHIEVING FIXATION. THE REMOVED SCREW WAS THEN REUSED IN A DIFFERENT BONE HOLE AND WAS FIXED WITHOUT ISSUE. NO IMPLANT COMPONENTS BROKE OFF INSIDE THE PATIENT, AND NO ADVERSE EFFECTS WERE REPORTED. THIS EVENT OCCURRED DURING A PROCEDURE ON (B)(6) 2025. ADDITIONAL INFORMATION WAS RECEIVED ON 08/15/2025: THIS EVENT OCCURRED DURING A DISTAL RADIUS FRACTURE REPAIR PROCEDURE ON (B)(6) 2025. A REPLACEMENT AR-8724V-22S LOW PROFILE VA LOCKING SCREW (LOT IS UNKNOWN) WAS INSERTED AFTER THE ORIGINAL SCREW PENETRATED THE PLATE AND WAS REMOVED. THERE WAS NO SIGNIFICANT DELAY TO THE PROCEDURE, AND NO ADDITIONAL ANESTHESIA WAS ADMINISTERED. IT WAS ALSO CONFIRMED THAT NO OTHER PRODUCTS WERE INVOLVED IN THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22883364 ↗
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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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