Arthrex® AR-8730-36HSRecalls & reported problems
Arthrex, Inc. · COMPR FT SCRW,3.5 MINI, 36mm · Class 2 · Implant
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 00888867303966), received between May 11, 2023 and May 11, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Material Fragmentation” (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.
Most reported problems
Device problems
- Material Fragmentation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 11, 2023Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT AFTER AN INITIAL ARTHRODESIS SURGERY FOR HALLUX RIGIDUS ON 22ND (B)(6)2022 THE PATIENT DEVELOPED AN GRANULOMA FORMATION. A SURGICAL EXPLORATION WAS PERFORMED AND A FRAGMENT OF THE SCREW WAS IDENTIFIED. AN ADDITIONAL SURGERY WAS PERFORMED ON (B)(6) 2023 TO PERFORM A FRESECTION OF THE GANULOMA.
Patient problems: Foreign Body In Patient
MAUDE report 16914538 ↗
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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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