BRONCHOVIDEOSCOPE BF-1T150 (UDI 04953170308185)Recalls & reported problems
Olympus Medical Systems Corp. · Class 2
All models of BRONCHOVIDEOSCOPE (8)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This Olympus BF-1T150 bronchovideoscope has 203 adverse event reports, with no deaths and no injuries. Common complaints include no display or image, peeling parts, and poor cleaning, and nearly all reports note no effect on patients. It has 4 open recalls about use with burning tools, airway burn risk, wet channels that could carry infection, and a scope that can lodge in a tube connector.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 212
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 4
Summary
The FDA's MAUDE database contains 212 adverse event reports that list this exact device (DI 04953170308185), received between Aug 23, 2018 and Sep 30, 2026 — classified as 212 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (47 reports).
4 FDA recall records name this device's identifier, 4 still open.
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.
Reports received per month
Recalls naming this device
- Sep 11, 2025Open, Classified
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Z-0045-2026 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 12, 2023Open, Classified
There is a risk of endobronchial combustion if high-frequency cauterization is performed while supplying oxygen [and/or] the electrode section of the electrosurgical accessory is too close to the distal end of the endoscope.
Z-0189-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 25, 2023Open, Classified
Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection
Z-0327-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Jul 27, 2023Open, Classified
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Z-2490-2023 · Root cause: Labeling Change Control · Recall details · FDA record ↗
Most reported problems
Device problems
- No Display/Image47
- Peeled/Delaminated39
- Failure to Clean Adequately17
- Poor Quality Image17
- Corroded16
- Erratic or Intermittent Display16
- Material Deformation15
- Detachment of Device or Device Component14
Patient problems
- No Clinical Signs, Symptoms or Conditions203
- No Consequences Or Impact To Patient8
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 25 most recent of 212 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Peeled/Delaminated; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953528 ↗MalfunctionSep 17, 2026Detachment of Device or Device Component; Material Deformation
The customer returned the Bronchovideoscope to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the Bronchovideoscope Connecting tube's coating was peeling 1mm2 or more and the forceps channel port had a dent. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50805809 ↗MalfunctionSep 16, 2026Dent in Material
The customer returned the bronchovideoscope to the service center for a separate issue. During the device analysis, it was indicated that a dent on the forceps channel port was found. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794835 ↗MalfunctionSep 14, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765635 ↗MalfunctionSep 10, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50724675 ↗MalfunctionSep 10, 2026Erratic or Intermittent Display
It was reported that the bronchoscope was not working properly (intermittent problem) occurred at Reprocessing involving an Olympus Bronchovideoscope. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50714239 ↗MalfunctionAug 29, 2026Corroded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50510197 ↗MalfunctionAug 28, 2026Corroded; Failure to Clean Adequately
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50502493 ↗MalfunctionAug 26, 2026Corroded; Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50464374 ↗MalfunctionAug 25, 2026Loss of or Failure to Bond; Scratched Material
It was observed that during the device evaluation, the broncho videoscope had detached bending section cover adhesive and a shaved forceps channel port. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50438282 ↗MalfunctionAug 19, 2026Corroded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50329125 ↗MalfunctionAug 19, 2026Detachment of Device or Device Component
No additional information received from the customer.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50328922 ↗MalfunctionAug 19, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50322689 ↗MalfunctionAug 13, 2026Device Reprocessing Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50243067 ↗MalfunctionAug 12, 2026Thermal Decomposition of Device
The customer returned the Bronchovideoscope to the service center for a separate issue. During the device analysis, the service repair technician indicates that the distal end had a burn. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50222843 ↗MalfunctionAug 12, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50217104 ↗MalfunctionAug 11, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50204673 ↗MalfunctionAug 7, 2026Detachment of Device or Device Component
The customer returned the BRONCHO VIDEOSCOPE to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the BRONCHO VIDEOSCOPE's bending section cover adhesive was detached near the distal end. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50183544 ↗MalfunctionAug 6, 2026Crack; Degraded; Material Fragmentation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50158900 ↗MalfunctionJul 31, 2026Thermal Decomposition of Device
The customer returned the Bronchovideoscope to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the Bronchovideoscope's distal end was burned. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50101536 ↗MalfunctionJul 30, 2026Material Fragmentation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50087014 ↗MalfunctionJul 30, 2026Material Fragmentation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50084686 ↗MalfunctionJul 27, 2026Thermal Decomposition of Device; Corroded
No additional information received from the customer.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50015685 ↗MalfunctionMay 18, 2026Thermal Decomposition of Device; Material Deformation
IT WAS REPORTED THE BRONCHO VIDEOSCOPE HAD TIP DAMAGE DUE TO A CAUTERY BURN. THE ISSUE WAS NOTED DURING SET UP IN ROOM / BEFORE PATIENT IN ROOM. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25210997 ↗MalfunctionApr 29, 2026Detachment of Device or Device Component
IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE BRONCHOVIDEOSCOPE WAS DELIVERED TO OLYMPUS WITHOUT THE RUBBER COVER. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25026685 ↗
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
- TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-DPOlympus Medical Systems Corp. · BRONCHOSCOPE (FLEXIBLE OR RIGID)1 recall332 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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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