Arthrex® AR-2652CLSRecalls & reported problems
Arthrex, Inc. · CLAV FRAC PLT,CENTRAL THIRD,LFT,SS, STRL · 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 00888867195912), received between Jul 13, 2021 and Jul 13, 2021 — classified as 1 malfunction.
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
- Material Twisted/Bent1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 13, 2021Break; Material Twisted/Bent
IT WAS REPORTED THAT THE DEVICE WAS IMPLANTED ON 11-MAY AND DURING A POST-OPERATIVE CHECK-UP AN X-RAY REVEALED, THAT THE DEVICE WAS ALREADY BEND A FEW DAYS AFTER THE SURGERY. ON 16-JUN THE DEVICE BROKE WHEN THE PATIENT WAS TYING HIS SHOES. A REVISION SURGERY WAS PERFORMED AND THE BROKEN DEVICE WAS REMOVED AND REPLACED WITH A DIFFERENT DEVICE. IN THE MEANTIME, THE HEALING OF THE FRACTURE ALREADY PROGRESSED AND NO FURTHER COMPLICATIONS OCCURRED.
Patient problems: Insufficient Information
MAUDE report 12163145 ↗
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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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