LungVision Tool Bridge (REF LV2055011)Recalls & reported problems
Body Vision Medical Ltd · The LungVision Tool is an instrument designed as a working channel intended to be used with standard bronchoscopes, endo-therapy accessories and ultrasound probe to guide the endo-therapy accessories or ultrasound probe to the target area, specifically within the respiratory system. LungVision Tool, LV2055011 is compatible with Olympus Bronchoscope BF-1TH190 LungVision Tool composed from: LungVision Handle, LungVision Adaptor with seal for Olympus Bronchoscope BF-1TH190, LungVision J Curved Sheath and LungVision Stylet · Class 2
Data updated Oct 18, 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 07290017652108), received between Mar 28, 2023 and Mar 28, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device 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
Device problems
- Use of Device Problem1
Patient problems
- Unspecified Respiratory Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 28, 2023Use of Device Problem; Use of Device Problem
LUNG BIOPSY WAS PERFORMED USING FORCEPS AND A BODYVISION LUNGVISION TOOL KIT ON (B)(6) 2023. THE PHYSICIAN DOES NOT RECALL ANY DIFFICULTIES OR IMMEDIATE COMPLICATIONS, NO SHARP ANGLES OF THE CATHETER AND NO DIFFICULTY ADVANCING THE TOOL. UPON COMPLETION OF THE BIOPSY PATHOLOGY, IT WAS DETERMINED THAT THERE WAS LUNG INFLAMMATION. THIS PATIENT, UNDERWENT AN ADDITIONAL PET SCAN AND IT WAS DETERMINED THAT ANOTHER LUNG BIOPSY WAS REQUIRED. DURING THIS ADDITIONAL BIOPSY PROCEDURE, THE PHYSICIAN FOUND RETAINED MATERIAL SUSPECTED TO BE FROM THE BODYVISION DEVICE. BODYVISION BECAME AWARE OF THIS EVENT ON MARCH 07, 2023.
Patient problems: Unspecified Respiratory Problem
MAUDE report 16626697 ↗
Other Bronchoscope (Flexible Or Rigid) devices
- EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190Olympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)3 recalls5 deaths1,557 reports
- EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190Olympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)4 recalls1 death1,214 reports
- EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-XP190Olympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)4 recalls1,146 reports
- Ion 380748Intuitive Surgical, Inc. · Bronchoscope (flexible or rigid)1 recall97 deaths1,278 reports
- VISERA ELITE XENON LIGHT SOURCE OLYMPUS CLV-S190Olympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)1,155 reports
- EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190Olympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)5 recalls3 deaths621 reports
- EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190Olympus Medical Systems Corp. · Bronchoscope (Flexible Or Rigid)3 recalls333 reports
- BRONCHOVIDEOSCOPE BF-1T150Olympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)4 recalls212 reports
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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