C2 CryoBalloon FG-1056Recalls & reported problems
Pentax Of America, Inc. · Class 2
Data updated Oct 18, 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 04961333255320), received between Oct 18, 2023 and Oct 18, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Firing 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.
Reports received per month
Most reported problems
Device problems
- Firing Problem1
- Unintended Movement1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 18, 2023Unintended Movement; Firing Problem; Unintended Movement; Firing Problem
PENTAX MEDICAL BECAME AWARE OF AN EVENT WHICH OCCURRED DURING A CLINICAL STUDY (PROTOCOL CP-0019 REV B) IN THE NETHERLANDS INVOLVING CRYOBALLOON ABLATION SYSTEM CONTROLLER MODEL FG-1017, FOOT PEDAL MODEL FG-1018, AND CATHETER MODEL FG-1056. CATHETER MODEL FG-1056 IS AN INVESTIGATIONAL CATHETER ESPECIALLY MANUFACTURED FOR THIS STUDY AND IS NOT AVAILABLE COMMERCIALLY. PER THE INITIAL REPORT, THE FIRST 180 DEGREE TREATMENT DURING THE PROCEDURE WENT AS INTENDED BY THE CLINICAL STUDY RESEARCH PHYSICIAN. THE PHYSICIAN PROCEEDED TO THE NEXT STEP OF THE PROCEDURE TO TREAT AN ADDITIONAL AREA OF THE ESOPHAGUS. THE PHYSICIAN USED THE FOOT PEDAL TO ROTATE THE DIFFUSER LOCATED WITHIN THE CATHETER BALLOON TO PLACE THE DIFFUSER IN POSITION TO TREAT THE NEXT SEGMENT OF UNWANTED TISSUE OF THE ESOPHAGUS. WHEN THE PHYSICIAN STOPPED PRESSING THE FOOT PEDAL, THE DIFFUSER CONTINUED TO ROTATE BEYOND THE INTENDED STOPPING POSITION. AT THIS POINT IN THE PROCEDURE, THE ENDOSCOPIST INTENDED TO USE THE FOOT PEDAL TO PRODUCE A SHORT BURST OF CRYO-TREATMENT (CALLED A PRE-PUFF) TO EVALUATE THE EXACT POSITION OF THE DIFFUSER IN THE ESOPHAGUS. THE ACTUAL PRE-PUFF WAS NOT AN EXPECTED SHORT BURST OF CRYO-TREATMENT;
Patient problems: Pain
MAUDE report 17959809 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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