Single Use Grasping Forceps FG-804LRecalls & reported problems
Olympus Medical Systems Corp. · Class 2
Data updated Oct 16, 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 04953170435874), received between Apr 27, 2023 and Apr 28, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Difficult to Open or Close” (2 reports).
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.
Most reported problems
Device problems
- Difficult to Open or Close2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 28, 2023Difficult to Open or Close; Difficult to Open or Close
THE CUSTOMER REPORTED TO OLYMPUS THAT THE SINGLE USE GRASPING FORCEPS FG-804L DID NOT OPEN WHILE IT WAS GRASPING THE GASTROJEJUNOSTOMY (GJ) TUBE IN THE MIDDLE OF A THERAPEUTIC PROCEDURE TO REPLACE A GJ TUBE. OTHER THAN CUTTING THE FORCEPS, PULLING IT OUT, AND CHECKING FOR ANY FOREIGN BODIES, NO OTHER INTERVENTION WAS DONE OUTSIDE THE PLANNED CASE. THE PROCEDURE WAS PROLONGED BY 30 MINUTES, TWICE AS LONG AS ANTICIPATED, WITH THE PATIENT UNDER ANESTHESIA. HOWEVER, THERE WERE NO OTHER COMPLICATIONS NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16829624 ↗InjuryApr 27, 2023Difficult to Open or Close; Difficult to Open or Close
THE CUSTOMER REPORTED TO OLYMPUS THAT THE SINGLE USE GRASPING FORCEPS FG-804L DID NOT OPEN WHILE IT WAS GRASPING THE GASTROSTOMY-JEJUNOSTOMY (GJ) TUBE IN THE MIDDLE OF A THERAPEUTIC PROCEDURE TO REPLACE A GJ TUBE. OTHER THAN CUTTING THE FORCEPS, PULLING IT OUT, AND CHECKING FOR ANY FOREIGN BODIES, NO OTHER INTERVENTION WAS DONE OUTSIDE THE PLANNED CASE. THE PROCEDURE WAS PROLONGED BY 30 MINUTES, TWICE AS LONG AS ANTICIPATED, WITH THE PATIENT UNDER ANESTHESIA. HOWEVER, THERE WERE NO OTHER COMPLICATIONS NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16827532 ↗
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- VIVIDEO VNL9-CPHoya Corporation · Nasopharyngoscope (Flexible Or Rigid)389 reports
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- SINGLE USE BIOPSY VALVE MAJ-210Olympus Medical Systems Corp. · Nasopharyngoscope (Flexible Or Rigid)1 recall221 reports
- SINGLE USE SUCTION VALVE MAJ-209Olympus Medical Systems Corp. · Nasopharyngoscope (Flexible Or Rigid)228 reports
- PENTAX FNL-7RP3Hoya Corporation · NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)227 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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