Tricut® 1882904Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20681490047269), received between Jun 14, 2018 and Aug 13, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 13, 2020Break; Material Separation; Break; Material Separation

  ADDITIONAL INFORMATION RECEIVED FROM MANUFACTURER REPRESENTATIVE STATING THAT THE TIP, JUST BELOW THE MOUTH OF THE BLADE BROKE OFF AND WAS RETRIEVED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10400276 ↗
• MalfunctionJun 14, 2018Break; Break

  THE SHAVER TRICUT BLADE 2.9MM WAS USED FOR AN ENDOSCOPIC TURBINOPLASTY. DURING THE PROCEDURE THE INNER BLADE BROKE OFF WHILE IN USE. THERE WERE NO EVIDENT PARTICLES IN THE PATIENT. THE TEAM ACTED QUICKLY AND CONTACTED THE RADIOGRAPHER TO COME TO THEATRE (OPERATING ROOM). MULTIPLE IMAGES WERE TAKEN FROM THE PATIENT¿S HEAD TO CHEST AND AT DIFFERENT ANGLES. THE INCIDENT OCCURRED NEAR THE END AND A NEW BLADE WAS OPENED TO COMPLETE THE PROCEDURE. THE TIME THE PATIENT WAS IN THEATRE WAS LENGTHENED. HOWEVER, THE PATIENT IS ALIVE AND WELL AND WAS INFORMED OF THE INCIDENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7603159 ↗