RHINO-LARYNGOFIBERSCOPERecalls & reported problems across all models
Olympus Medical Systems Corp. · 9 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name at least one RHINO-LARYNGOFIBERSCOPE model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 188
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 2
We found 9 models of RHINO-LARYNGOFIBERSCOPE by Olympus Medical Systems Corp. in the FDA's device registry (GUDID). Together they are named in 188 adverse event reports in the FDA's MAUDE database, received between Jan 15, 2020 and Sep 30, 2026 — classified as 2 injuries, 186 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (45 reports).
2 FDA recall records name at least one of these models by its device identifier, 2 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-LARYNGOFIBERSCOPE 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.
- Dec 4, 2023Class IIOpen, Classified
Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
Z-0688-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- 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 · Recall details · FDA record ↗
Most reported RHINO-LARYNGOFIBERSCOPE problems
Device problems
- Detachment of Device or Device Component45
- Failure to Clean Adequately34
- Device Reprocessing Problem26
- Peeled/Delaminated22
- Break21
- Corroded10
- Loss of or Failure to Bond8
- Material Separation6
Patient problems
- No Clinical Signs, Symptoms or Conditions182
- No Consequences Or Impact To Patient3
- No Patient Involvement3
- Injury1
RHINO-LARYNGOFIBERSCOPE models
9 models, most reported first. Each model has its own page with its reports, recalls and device details.
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE XPNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)1 recall29 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE GPNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)77 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF-T3NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)1 recall9 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE P4NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)51 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE P4Nasopharyngoscope (flexible or rigid)11 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF-T3NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)5 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE GPNASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)2 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF-T3Nasopharyngoscope (flexible or rigid)2 reports
- RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE XPNasopharyngoscope (Flexible Or Rigid)2 reports
Recent RHINO-LARYNGOFIBERSCOPE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Corroded
The customer reported the Rhino-Laryngo Videoscope had a separate issue. During the initial evaluation of the device, it was observed that the connector lens was corroded. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947115 ↗MalfunctionSep 24, 2026Device Reprocessing Problem
The customer reported the Rhino-Laryngo fiberscope had a separate issue. During the initial evaluation of the device it was observed, that the eyepiece had dirt on it. No patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885230 ↗MalfunctionSep 21, 2026Failure to Clean Adequately
It was observed that during the device inspection, the Rhino-Laryngofiberscope exhibited the LG-cover glass had foreign objects. There were no reports of patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50835130 ↗MalfunctionSep 18, 2026Detachment of Device or Device Component
The customer reported there was an unprotected Distal Tip during reprocessing. The issue involved an Olympus Rhino Laryngofiberscope. Additionally, during the initial device analysis, the Olympus Service Repair Technician indicated that the Insertion Section Distal rubber was detached. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50818804 ↗MalfunctionSep 16, 2026Peeled/Delaminated
The customer reported that the Rhino-Laryngo fiberscope had peeled off coating during inspection for use. During the initial evaluation of the device, it was also observed that the coating was peeled. No patient harm was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50793154 ↗MalfunctionSep 16, 2026Corroded
The customer returned the Rhino Laryngofiberscope to the service center for a separate issue. During the device analysis, it was indicated that a corroded distal end was found. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50791172 ↗MalfunctionSep 11, 2026Device Reprocessing Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50737639 ↗MalfunctionSep 4, 2026Corroded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50623729 ↗MalfunctionSep 2, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50576590 ↗MalfunctionAug 31, 2026Peeled/Delaminated
It was observed that during the device evaluation, the rhino-laryngofiberscope insertion tube coating was peeled off. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50525103 ↗MalfunctionAug 26, 2026Break; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50455667 ↗MalfunctionAug 14, 2026Detachment of Device or Device Component
The customer reported the tip of the Olympus Rhino-Laryngofiberscope had come apart. The issue was identified during reprocessing. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50251317 ↗MalfunctionAug 13, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50234514 ↗MalfunctionAug 11, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50201932 ↗MalfunctionAug 10, 2026Device Reprocessing Problem
The customer returned the rhino-laryngofiberscope to the service center for a separate issue. During the device analysis, It was indicated that dirt deposition in the bending section cover and connecting tube was found. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50195863 ↗
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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