Arthrex® AR-18710-10Recalls & reported problems
Arthrex, Inc. · Low Profile Screw, 1.0x10mm, Cortical,Ti · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867303607), received between Apr 28, 2025 and Sep 9, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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
- Break2
Patient problems
- Foreign Body In Patient1
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2025Break; Break
ON (B)(6) 2025, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-18710-10 LOW PROFILE SCREW BROKE WHILE BEING IMPLANTED. THIS WAS DISCOVERED DURING THE CASE WITH NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23004780 ↗MalfunctionApr 28, 2025Break; Break
ON (B)(6) 2025, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT TWO AR-18710 CORTICAL SCREW HEAD BROKE OFF. THE SCREWS WERE TIGHTENED WITH 2-FINGER TIGHTNESS AND BROKE AS THE HEAD OF THE SCREW WAS MAKING CONTACT WITH THE CORTICAL BONE. THERE WAS NO PLATE USED DURING THE PROCEDURE. THE SURGEON LOCATED THE HEADS OF THE SCREWS AND WAS ABLE TO REMOVE THEM SUCCESSFULLY. THIS WAS DISCOVERED DURING A METACARPAL FRACTURE PROCEDURE ON (B)(6) 2025. ADDITIONAL INFORMATION REQUESTED ON 4/24/2025.
Patient problems: Foreign Body In Patient; Insufficient Information
MAUDE report 21917191 ↗
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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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