--- title: "Aizu Olympus Co., Ltd. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Aizu Olympus Co., Ltd. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/aizu-olympus-co-ltd/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Aizu Olympus Co., Ltd. recall records **30** reported ongoing 31 records in this archive. Latest source date Oct 31, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Oct 31, 2025 FDA device enforcement ### [Olympus OER-Elite](https://isitonrecall.com/recall/fda-device-z-0872-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Olympus OER-Elite](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0872-2026%22) Oct 31, 2025 FDA device enforcement ### [Olympus OER-Pro](https://isitonrecall.com/recall/fda-device-z-0873-2026-olympus-oer-pro/) Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Olympus OER-Pro](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0873-2026%22) Oct 31, 2025 FDA device enforcement ### [Olympus OER-Mini](https://isitonrecall.com/recall/fda-device-z-0874-2026-olympus-oer-mini/) Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Olympus OER-Mini](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0874-2026%22) Oct 16, 2023 FDA device enforcement ### [CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE](https://isitonrecall.com/recall/fda-device-z-0415-2024-cf-hq190l-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 impact the ability to effectively reproc... Class II Reported ongoing Distribution: Domestic distribution to FL, KY, MA, NJ, NY, and PA [Official source for CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0415-2024%22) Oct 16, 2023 FDA device enforcement ### [GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE](https://isitonrecall.com/recall/fda-device-z-0416-2024-gif-h190-evis-exera-iii-gastrointestinal-videoscope/) 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 reproc... Class II Reported ongoing Distribution: Domestic distribution to FL, KY, MA, NJ, NY, and PA [Official source for GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0416-2024%22) Oct 16, 2023 FDA device enforcement ### [GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE](https://isitonrecall.com/recall/fda-device-z-0417-2024-gif-hq190-evis-exera-iii-gastrointestinal-videoscope/) 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 reproc... Class II Reported ongoing Distribution: Domestic distribution to FL, KY, MA, NJ, NY, and PA [Official source for GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0417-2024%22) Oct 16, 2023 FDA device enforcement ### [PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE](https://isitonrecall.com/recall/fda-device-z-0418-2024-pcf-h190dl-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 impact the ability to effectively reproc... Class II Reported ongoing Distribution: Domestic distribution to FL, KY, MA, NJ, NY, and PA [Official source for PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0418-2024%22) Oct 16, 2023 FDA device enforcement ### [PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE](https://isitonrecall.com/recall/fda-device-z-0419-2024-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 impact the ability to effectively reproc... Class II Reported ongoing Distribution: Domestic distribution to FL, KY, MA, NJ, NY, and PA [Official source for PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0419-2024%22) Sep 25, 2023 FDA device enforcement ### [Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. Model Numbers: BF-1T150, BF-1T60, BF-1TH190, BF-1TQ170, BF-3C160, BF-3C40, BF-H19...](https://isitonrecall.com/recall/fda-device-z-0327-2024-bronchoscope-for-endoscopy-and-endoscopic-surgery-within-the-airways-and-tracheobronchial-tree-model/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. M...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0327-2024%22) Sep 25, 2023 FDA device enforcement ### [Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspiration and other endoscopic procedures within the airways, trancheobronchial tre...](https://isitonrecall.com/recall/fda-device-z-0328-2024-bronchoscope-ultrasonic-endoscopic-real-time-ultrasonic-imaging-ultrasound-guided-needle-aspiration/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0328-2024%22) Sep 25, 2023 FDA device enforcement ### [Colonoscope: for endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon and ileocecal valve). Model Numbers: CF-2T16...](https://isitonrecall.com/recall/fda-device-z-0329-2024-colonoscope-for-endoscopy-and-endoscopic-surgery-within-the-lower-digestive-tract-including-the-anus/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Colonoscope: for endoscopy and endoscopic surgery within the lower digestive tract (including the...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0329-2024%22) Sep 25, 2023 FDA device enforcement ### [Choleodochoscope. Model Numbers: CHF-BP30, CHF-CB30L, CHF-P60.](https://isitonrecall.com/recall/fda-device-z-0330-2024-choleodochoscope-model-numbers-chf-bp30-chf-cb30l-chf-p60/) 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 inf... Class III Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Choleodochoscope. Model Numbers: CHF-BP30, CHF-CB30L, CHF-P60.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0330-2024%22) Sep 25, 2023 FDA device enforcement ### [Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.](https://isitonrecall.com/recall/fda-device-z-0331-2024-cystonephroscope-endoscopic-diagnosis-and-treatment-within-the-bladder-urethra-and-kidney-model-numb/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0331-2024%22) Sep 25, 2023 FDA device enforcement ### [Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anatomy (including nasopharyngeal and trachea). Model Numbers: ENF-T3, ENF-VT2, ENF-VT3.](https://isitonrecall.com/recall/fda-device-z-0332-2024-rhinolaryngoscope-for-endoscopic-diagnosis-and-treatment-within-the-nasal-lumens-and-airway-anatomy/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anato...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0332-2024%22) Sep 25, 2023 FDA device enforcement ### [Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA) and for endoscopic surgery within the upper digestive tract. Model Numbers: GF-UC140P-AL5, GF-UCT180,...](https://isitonrecall.com/recall/fda-device-z-0333-2024-gastroscope-endoscopic-ultrasound-eus-guided-fine-needle-aspiration-fna-and-for-endoscopic-surgery-w/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA) and for endoscopic su...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0333-2024%22) Sep 25, 2023 FDA device enforcement ### [Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160...](https://isitonrecall.com/recall/fda-device-z-0334-2024-gastrointestinal-videoscope-indicated-for-use-within-the-upper-digestive-tract-including-the-esophag/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the eso...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0334-2024%22) Sep 25, 2023 FDA device enforcement ### [Hysteroscope-For endoscopic diagnosis within the uterus Model Number: HYF-1T.](https://isitonrecall.com/recall/fda-device-z-0335-2024-hysteroscope-for-endoscopic-diagnosis-within-the-uterus-model-number-hyf-1t/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Hysteroscope-For endoscopic diagnosis within the uterus Model Number: HYF-1T.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0335-2024%22) Sep 25, 2023 FDA device enforcement ### [Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V.](https://isitonrecall.com/recall/fda-device-z-0336-2024-hysterovideoscope-for-endoscopic-diagnosis-within-the-uterus-model-number-hyf-v/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0336-2024%22) Sep 25, 2023 FDA device enforcement ### [Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number: HYF-XP.](https://isitonrecall.com/recall/fda-device-z-0337-2024-hysterofiberscope-for-endoscopic-diagnosis-within-the-uterus-model-number-hyf-xp/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number: HYF-XP.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0337-2024%22) Sep 25, 2023 FDA device enforcement ### [Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: LF-DP, LF-GP, LF...](https://isitonrecall.com/recall/fda-device-z-0338-2024-tracheal-fiberscope-airway-management-which-includes-observation-to-access-airway-anatomy-endotrache/) 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 inf... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endot...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0338-2024%22) ## Reasons in these listed records - Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance. - 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... - 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 These examples come from this result page and are not a ranking of every recall reason. ## Checking Aizu Olympus Co., Ltd. ### Is there a recall on aizu olympus co., ltd. right now? This archive contains 31 records, including 30 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Aizu Olympus Co., Ltd.](https://isitonrecall.com/check/?q=Aizu%20Olympus%20Co.%2C%20Ltd.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)