Arthrex® AR-18724P-23Recalls & reported problems
Arthrex, Inc. · V- Plate, 2.4mm, 6 Hole · 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 00888867314429), received between Sep 14, 2023 and Sep 14, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fitting Problem” (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
- Fitting Problem1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2023Fitting Problem; Fitting Problem
ON (B)(6) 2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA PHONE THAT AN AR-18724P-23 V-PLATE HOLE EXPANDED AND THE SCREW WENT THROUGH THE PLATE. THIS WAS DISCOVERED DURING A CASE WITH NO PATIENT EFFECT. DELAY FROM PROCEDURE AROUND 15 MINUTES. CASE COMPLETED USING ANOTHER PLATE AND LARGER SCREW.
Patient problems: Failure of Implant
MAUDE report 17743413 ↗
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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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