Aizu Olympus recalls
4 official recalls and safety alerts involving Aizu Olympus since 2022-08, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Aizu Olympus or the relevant agency.
- 2025-12-10
US
Aizu Olympus Co., Ltd. recalls Olympus OER-Elite
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- 2023-12-06
US
Aizu Olympus Co., Ltd. recalls PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
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…
FDA · DeviceAizu Olympus Co., Ltd.Domestic distribution to FL, KY, MA, NJ, NY, and PAOfficial notice →- 2023-11-29
US
Aizu Olympus Co., Ltd. recalls Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum and sigmoid colon).…
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…
- 2022-08-31
US
Aizu Olympus Co., Ltd. recalls EVIS EXERA III Bronchovideoscope
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
FDA · DeviceAizu Olympus Co., Ltd.US Nationwide distribution in the states of FL, IL, NC, PA & TX.Official notice →