Arthrex® AR-1555CDSRecalls & reported problems
Arthrex, Inc. · BIO-COMP-TENOD SCRW W/DISP DRV 5.5X15MM · 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 00888867095175), received between Dec 2, 2022 and Dec 2, 2022 — 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
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 2, 2022Break
IT WAS REPORTED ON 11/16/2022 BY A ARTHREX EMPLOYEE VIA E-MAIL THAT AN AR-1555CDS BIO-COMPOSITE-TENODESIS FIBER WIRE THE TIP WAS CUT OFF DURING INSERTION AND THE GRAFT COULD NOT BE FIXED. A NEW PRODUCT WAS USED TO COMPLETE THE CASE. THIS OCCURRED ON (B)(6) 2022 DURING A PROCEDURE, WITH NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15905281 ↗
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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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