Class II
Medical Device Recall: Olympus Gastrointestinal Videoscope, Model/Catalog Number: GIF-1100
Olympus Corporation of the Americas · August 21, 2024
Reason for Recall
It was discovered during device performance testing that the CCD imaging sensors were programmed with the incorrect color correction data and therefore, specifications are not met.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
1407 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0181-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.