Arthrex® AR-2655CRSRecalls & reported problems
Arthrex, Inc. · CLAV FRAC PLT,CENTRAL THIRD,RT,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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867195899), received between Sep 10, 2020 and Sep 10, 2020 — 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
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.
InjurySep 10, 2020Break
IT WAS REPORTED THAT APPROX. 3 WEEKS POST OP, A CLAVICULA PLATE BROKE AND NEEDED TO BE REPLACED DURING A REVISION SURGERY. UPDATE 25-AUG-2020: PATIENT DID NOT SUFFER FROM A TRAUMA. THE BROKEN ARTHREX PLATE WAS REPLACED BY A PLATE FROM ANOTHER MANUFACTURER. PART NUMBERS OF THE SCREWS ARE UNKNOWN. THEY WILL NOT BE RETURNED FOR EVALUATION. INITIAL SURGERY WAS ON (B)(6) 2020, REVISION SURGERY WAS ON (B)(6) 2020.
Patient problems: Insufficient Information
MAUDE report 10513496 ↗
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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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