Beamer Plus CB200Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04057607000113), received between Jan 22, 2018 and Jan 22, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Gas/Air Leak” (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

Recent adverse event reports

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

• InjuryJan 22, 2018Gas/Air Leak; Gas/Air Leak

  THE USER FACILITY REPORTED THAT DURING SURGERY, THE CB200 BEAMER PLUS ARGON'S VALVE MALFUNCTIONED CAUSING ARGON GAS TO LEAK. THE DOCTOR HAD TO USE A SNARE TIP TO CAUTERIZE. THE PROCEDURE WAS COMPLETED WITH NO REPORTED PROCEDURAL DELAYS. THE PATIENT EXPERIENCED POLYPECTOMY SYNDROME AND REQUIRED ANTIBIOTIC TREATMENT. TO DATE, ALTHOUGH MULTIPLE ATTEMPTS HAVE BEEN MADE TO GATHER INFORMATION, NO ADDITIONAL INFORMATION REGARDING THE CURRENT PATIENT STATUS AND PROCEDURE HAS BEEN MADE AVAILABLE.

  Patient problems: Fever; Unspecified Infection

  MAUDE report 7208977 ↗