RHINO-LARYNGO VIDEOSCOPERecalls & reported problems across all models
Olympus Medical Systems Corp. · 15 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one RHINO-LARYNGO VIDEOSCOPE model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 623
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls
- 1
We found 15 models of RHINO-LARYNGO VIDEOSCOPE by Olympus Medical Systems Corp. in the FDA's device registry (GUDID). Together they are named in 623 adverse event reports in the FDA's MAUDE database, received between Aug 13, 2019 and Sep 30, 2026 — classified as 4 injuries, 619 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (172 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
RHINO-LARYNGO VIDEOSCOPE recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Sep 25, 2023Class IIOpen, 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-0332-2024 · Root cause: Under Investigation by firm · names 2 of these models · Recall details · FDA record ↗
Most reported RHINO-LARYNGO VIDEOSCOPE problems
Device problems
- Detachment of Device or Device Component172
- Failure to Clean Adequately85
- Device Reprocessing Problem81
- Peeled/Delaminated61
- Material Fragmentation42
- Break28
- Crack21
- Material Split, Cut or Torn21
Patient problems
- No Clinical Signs, Symptoms or Conditions612
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available3
- Insufficient Information3
- Discomfort1
- Foreign Body In Patient1
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
- Unspecified Tissue Injury1
RHINO-LARYNGO VIDEOSCOPE models
15 models, most reported first. Each model has its own page with its reports, recalls and device details.
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-V3Nasopharyngoscope (flexible or rigid)150 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-VHNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)118 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-VHEndoscope, accessories, narrow band spectrum87 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF TYPE VT2BRONCHOSCOPE (FLEXIBLE OR RIGID)1 recall33 reports
- RHINO-LARYNGO VIDEOSCOPE ENF-VT3Nasopharyngoscope (Flexible Or Rigid)1 recall23 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-V3NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)62 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF TYPE VQBRONCHOSCOPE (FLEXIBLE OR RIGID)46 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-VHNasopharyngoscope (Flexible Or Rigid)38 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-V4Endoscope, accessories, narrow band spectrum28 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-VH2Endoscope, accessories, narrow band spectrum22 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF TYPE VQEndoscope, accessories, narrow band spectrum8 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-VT3Endoscope, accessories, narrow band spectrum3 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-V4Nasopharyngoscope (flexible or rigid)2 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF TYPE VT2Endoscope, accessories, narrow band spectrum2 reports
- RHINO-LARYNGO VIDEOSCOPE OLYMPUS ENF-VH2Nasopharyngoscope (flexible or rigid)1 report
Recent RHINO-LARYNGO VIDEOSCOPE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Peeled/Delaminated
The customer returned the videoscope to the service center for evaluation of a separate issue. During the evaluation, a reportable malfunction was identified: coating peeling on the insertion tube. The affected component required replacement. There was no patient involvement associated with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951334 ↗MalfunctionSep 29, 2026Peeled/Delaminated
The customer returned the videoscope, an Olympus asset with no reported complaint. During the evaluation of the device, it was observed that the A-rubber was missing. The affected component required replacement. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936083 ↗MalfunctionSep 25, 2026Contamination; Detachment of Device or Device Component
The customer returned the Rhino-Laryngo Videoscope to the service center for a separate issue. During the device analysis, the Olympus Service Repair Technician indicated that there was foreign material on the Objective Lens and the Distal Sheath was detached. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50896484 ↗MalfunctionSep 25, 2026Contamination
The customer returned the Rhino Laryngo Videsocope to the service center for a separate issue. During the device analysis, the Olympus Service Repair Technician indicated that there was a dirty Objective Lens and a dirty Distal Sheath glue. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50896259 ↗MalfunctionSep 24, 2026Detachment of Device or Device Component
The customer returned the videoscope to the service center for evaluation of a separate issue. During the evaluation, a reportable malfunction was identified: missing A-rubber. The affected component required replacement. No patient involvement was associated with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50883355 ↗MalfunctionSep 23, 2026Peeled/Delaminated
The customer reported that the Rhino-Laryngo Videoscope had a peeled scope tip. There were no reports of patient harm.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870055 ↗MalfunctionSep 23, 2026Detachment of Device or Device Component
During onsite inspection of the Rhino-Laryngo Videoscope it was found that the adhesive glue was missing. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50863504 ↗MalfunctionSep 23, 2026Peeled/Delaminated
The customer returned the VIdeoscope to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the VIdeoscope's insertion tube coating was peeling. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50863377 ↗MalfunctionSep 23, 2026Detachment of Device or Device Component
The customer returned the Videoscope to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the Videoscope was missing glue around the objective lens. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50863376 ↗MalfunctionSep 22, 2026Material Fragmentation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50862408 ↗MalfunctionSep 22, 2026Detachment of Device or Device Component
The customer returned the videoscope which is an Olympus asset with no reported complaint. During evaluation, the A-rubber was found to be missing. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50857554 ↗MalfunctionSep 22, 2026Detachment of Device or Device Component
The customer returned the Videoscope to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the Videoscope's objective lens had chipped adhesive. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50849852 ↗MalfunctionSep 21, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50848768 ↗MalfunctionSep 21, 2026Corroded
The customer returned the Rhino-Laryngo Videoscope to the service center for evaluation related to a separate issue. During testing, the service repair technician identified the device ETO valve (venting connector) is corroded. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50846217 ↗MalfunctionSep 17, 2026Material Fragmentation
The customer returned the Videoscope to the service center for a separate issue. During Olympus¿ device analysis it was indicated that the Videoscope distal end was was chipped near the light guide lens. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50805843 ↗
Other Olympus Medical Systems Corp. products
- EVIS EXERA lll COLONOVIDEOSCOPE16 models · 15,013 reports · 7 recalls
- EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE7 models · 13,448 reports · 7 recalls
- EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE9 models · 8,317 reports · 2 recalls
- EVIS EXERA III BRONCHOVIDEOSCOPE11 models · 6,060 reports · 16 recalls
- EVIS EXERA III XENON LIGHT SOURCE2 models · 6,694 reports
- EVIS EXERA III COLONOVIDEOSCOPE6 models · 6,117 reports · 5 recalls
- EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V2 models · 5,281 reports · 4 recalls
- HD CAMERA HEAD2 models · 5,217 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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