Arthrex® AR-2262Recalls & reported problems
Arthrex, Inc. · BUTTON INSERTER · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867026490), received between Aug 1, 2022 and Aug 1, 2022 — classified as 1 injury.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Nerve Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 1, 2022Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED ON 07/11/2022 BY A FACILITY REPRESENTATIVE VIA PHONE THAT AN AR-7234 FIBERLOOP, AR-2261 BICEPS BUTTON AR-2262 BUTTON INSERTER AND AR-2263 DRILL WERE INVOLVED IN A DISTAL BICEPS REPAIR, THE PATIENT SUFFERED A CONTINUING NERVE ISSUE AFTER THE SURGERY. REVISION SURGERY (B)(6) 2022 TO REMOVE BUTTON AND PUT IN ANCHOR.
Patient problems: Nerve Damage
MAUDE report 15137731 ↗
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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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