Silicone connection set for tracheal intubation scopes OLYMPUS LF-GP/DP/TP OO LFRecalls & reported problems
Plasmabiotics · Silicone connection set for tracheal intubation scopes OLYMPUS LF-GP/DP/TP · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03701354402003), received between Jul 25, 2022 and Jul 25, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
- Loss of or Failure to Bond1
- Material Separation1
Patient problems
- Foreign Body In Patient2
- Obstruction/Occlusion1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 25, 2022Material Separation; Material Separation
THE CUSTOMER REPORTS DURING AN UNSPECIFIED THORACIC PROCEDURE USING A LF-GP FIBERSCOPE, HAD A PIECE OF THE INSERTION TUBE BREAK OFF INTO THE PATIENT'S LARYNX DURING A PROCEDURE AND HAD TO BE RETRIEVED. THE INTENDED PROCEDURE WAS COMPLETED. NO FURTHER CONSEQUENCES TO THE PATIENT HAVE BEEN REPORTED. ADDITIONAL DETAILS REGARDING THE PATIENT AND REPORTED EVENT HAVE BEEN REQUESTED. AT THIS TIME, NO ADDITIONAL INFORMATION HAS BEEN PROVIDED. THE DEVICE WAS RETURNED TO OLYMPUS FOR EVALUATION. THE INSERTION PORTION WAS INSPECTED UNDER A MICROSCOPE AND FOUND APPROXIMATELY 50 PERCENT OF THE BEND SECTION COVER GLUE WAS DETACHED ON THE INSERTION TUBE SIDE. THE MISSING PORTION WAS RETURNED WITH THE PHYSICAL DEVICE.
Patient problems: Foreign Body In Patient
MAUDE report 15095585 ↗InjuryJul 25, 2022Loss of or Failure to Bond; Detachment of Device or Device Component
THE CUSTOMER REPORTS DURING AN UNSPECIFIED THORACIC PROCEDURE USING A LF-GP FIBERSCOPE, HAD A PIECE OF THE INSERTION TUBE BREAK OFF INTO THE PATIENT'S LARYNX DURING A PROCEDURE AND HAD TO BE RETRIEVED. THE INTENDED PROCEDURE WAS COMPLETED. NO FURTHER CONSEQUENCES TO THE PATIENT HAVE BEEN REPORTED. ADDITIONAL DETAILS REGARDING THE PATIENT AND REPORTED EVENT HAVE BEEN REQUESTED. AT THIS TIME, NO ADDITIONAL INFORMATION HAS BEEN PROVIDED. THE DEVICE WAS RETURNED TO OLYMPUS FOR EVALUATION. THE INSERTION PORTION WAS INSPECTED UNDER A MICROSCOPE AND FOUND APPROXIMATELY 50 PERCENT OF THE BEND SECTION COVER GLUE WAS DETACHED ON THE INSERTION TUBE SIDE. THE MISSING PORTION WAS RETURNED WITH THE PHYSICAL DEVICE
Patient problems: Foreign Body In Patient; Obstruction/Occlusion
MAUDE report 15095583 ↗
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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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