Arthrex® AR-8735BV-20Recalls & reported problems
Arthrex, Inc. · 3.5x20mm Beveled FT Screw · 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 00888867360655), received between Nov 1, 2024 and Nov 1, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
- Material Protrusion/Extrusion1
Patient problems
- Foreign Body In Patient1
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 1, 2024Device Dislodged or Dislocated; Material Protrusion/Extrusion; Device Dislodged or Dislocated; Material Protrusion/Extrusion
ON 10/18/2024, IT WAS REPORTED BY A FACILITY REPRESENTATIVE THAT A PATIENT WHO WAS PART OF THE CLINICAL RESEARCH STUDY RETURNED FOR A MONTH'S VISIT, IN WHICH IT WAS FOUND THAT THE FRACTURE HAD SUBSIDED, AND THE AR-8735BV-20 BEVELED FT SCREW WAS PROTRUDING INTO THE MCP JOINT SPACE. IT WAS DETERMINED THAT REMOVING THE SCREW WAS THE NEXT STEP. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Foreign Body In Patient; Implant Pain
MAUDE report 20586774 ↗
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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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