Suction Irrigation Cartridge Set C7100Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00607915127589), received between Mar 8, 2016 and Mar 8, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Retraction Problem” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 8, 2016Retraction Problem; Retraction Problem

  LAPAROSCOPIC CHOLECYSTECTOMY - "SUCTION CONTROL STUCK IN THE ON POSITION. UNABLE TO DISENGAGE THE FINGER CONTROL. SUCTION RAN CONTINUOUSLY WHEN NOT BEING USED. TRIED PRESSING BOTH BUTTONS, ALTERNATING BUTTONS, PRYING THE BUTTON UP, AND TURNING PUMP AND SUCTION OFF AND BACK ON WITH NO SUCCESS. HAD USED APPROPRIATELY 500 MLS OF SALINE AT THE POINT THAT THE BUTTON STUCK. ULTIMATELY THE BUTTON DID SHUT OFF, BUTT WE DON'T KNOW WHAT FIXED IT." PATIENT STATUS - "PATIENT WAS CHARGED FOR A SECOND DEVICE." TYPE OF INTERVENTION - "A NEW SUCTION DEVICE WAS OPENED DUE TO THE UNRELIABILITY OF THE STUCK BUTTON."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 5488037 ↗