Arthrex® AR-13326Recalls & reported problems
Arthrex, Inc. · SCREWDRIVER 3,5 MM HEX · 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 00888867011380), received between Sep 19, 2018 and Sep 19, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
- Detachment of Device or Device Component1
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.
InjurySep 19, 2018Break; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING AN OSTEOTOMY OF TIBIA + LCA PROCEDURE, THE TIP OF THE 3.5MM HEX SCREWDRIVER BROKE OFF AS THE SURGEON WAS MANUALLY TIGHTENING THE SCREW. THE TIP OF THE DRIVER WAS NOT ABLE TO BE RETRIEVED. THE SURGEON SWITCHED TO A DRIVER FROM ANOTHER MANUFACTURER TO COMPLETE THE CASE WITH NO FURTHER INCIDENT.
Patient problems: Foreign Body In Patient
MAUDE report 7888792 ↗
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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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