Aizu Olympus Co., Ltd.
3-1-1 Niiderakita, AIZUWAKAMATSU-SHI Fukushima, JP
Registered product codes
28 product codes
Recent MDR events
159,966 on file
- EVIS EXERA III COLONOVIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61741
- EVIS LUCERA DUODENOVIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61756
- EVIS EXERA III COLONOVIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61757
- EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61758
- EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61759
- EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61760
- GASTROINTESTINAL VIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61761
- EVIS EXERA III COLONOVIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61762
- EVIS LUCERA GASTROINTESTINAL VIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61763
- GASTROINTESTINAL VIDEOSCOPEJul 31, 2026Malfunction9610595-2026-61764
Recalls
31 on file
- Open, ClassifiedDec 2, 2025
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
View FDA record ↗ - Open, ClassifiedDec 2, 2025
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
View FDA record ↗ - Open, ClassifiedDec 2, 2025
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
View FDA record ↗ - Open, ClassifiedNov 29, 2023
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
View FDA record ↗ - Open, ClassifiedNov 29, 2023
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
View FDA record ↗ - Open, ClassifiedNov 29, 2023
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
View FDA record ↗ - Open, ClassifiedNov 29, 2023
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
View FDA record ↗ - Open, ClassifiedNov 29, 2023
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
View FDA record ↗ - Open, ClassifiedNov 17, 2023
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
View FDA record ↗ - Open, ClassifiedNov 17, 2023
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
View FDA record ↗
Compliance history
Matched by FEI 3002964398.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
20 on file
Top refusal reasons
Compare to industry ↗- Division of Southeast Imports (DSEI)Jan 26, 2026
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)
- Division of Southeast Imports (DSEI)Oct 28, 2025
78FGB \ URETEROSCOPE
- Division of West Coast Imports (DWCI)Aug 12, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Aug 7, 2025
80FEB \ ACCESSORIES, CLEANING, FOR ENDOSCOPE
- Division of Northeast Imports (DNEI)Aug 7, 2025
80FEB \ ACCESSORIES, CLEANING, FOR ENDOSCOPE
- Division of Northeast Imports (DNEI)Aug 6, 2025
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)
- Division of Northeast Imports (DNEI)Aug 6, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Aug 5, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Aug 5, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Aug 5, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Aug 5, 2025
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)
- Division of Northeast Imports (DNEI)Aug 5, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Aug 5, 2025
78FGB \ URETEROSCOPE
- Division of Southeast Imports (DSEI)Jul 29, 2025
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)
- Division of Northeast Imports (DNEI)Jul 28, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Jul 28, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Jul 28, 2025
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)
- Division of Northeast Imports (DNEI)Jul 28, 2025
78FGB \ URETEROSCOPE
- Division of Northeast Imports (DNEI)Jul 28, 2025
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)
- Division of Northeast Imports (DNEI)Jul 28, 2025
77EOQ \ BRONCHOSCOPE (FLEXIBLE OR RIGID)