--- title: "Karl Storz Endoscopy Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Karl Storz Endoscopy recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/karl-storz-endoscopy/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Karl Storz Endoscopy recall records **52** reported ongoing 52 records in this archive. Latest source date May 21, 2026. 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 May 21, 2026 FDA device enforcement ### [Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF: 26153EAU/1.](https://isitonrecall.com/recall/fda-device-z-2794-2026-flexible-hystero-fiberscope-kits-ref-11264bbu1-11264bbuk1-that-contain-expired-single-use-endoscopic/) Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact the assurance of sterility. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, MA, MN, TX, OH, NY, CA, MI, LA, VA, MD, PA, GA, WI, VT. [Official source for Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2794-2026%22) Dec 19, 2024 FDA device enforcement ### [Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE](https://isitonrecall.com/recall/fda-device-z-0837-2025-karl-storz-endoskope-ref-723400-optical-biopsy-and-grasping-forceps-ce/) Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance. Class II Reported ongoing Distribution: US: AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OR, PA, SC, TX, VA OUS: None [Official source for Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0837-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27003L, MICHEL Uretero-Renoscope, 9.5 Fr., 43cm, RxONLY, CE0123](https://isitonrecall.com/recall/fda-device-z-1051-2025-karl-storz-endoskope-ref-27003l-michel-uretero-renoscope-9-5-fr-43cm-rxonly-ce0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27003L, MICHEL Uretero-Renoscope, 9.5 Fr., 43cm, RxONLY, CE0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1051-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE](https://isitonrecall.com/recall/fda-device-z-1052-2025-karl-storz-endoskope-ref-27030ka-cysto-urethroscope-non-sterile-ce/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1052-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27030KB, Pediatric Cysto-Urethroscope, NON STERILE, CE](https://isitonrecall.com/recall/fda-device-z-1053-2025-karl-storz-endoskope-ref-27030kb-pediatric-cysto-urethroscope-non-sterile-ce/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27030KB, Pediatric Cysto-Urethroscope, NON STERILE, CE](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1053-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27002KP, Pediatric Uretero-Renoscope 7.3 Fr., NON STERILE, CE 0123](https://isitonrecall.com/recall/fda-device-z-1054-2025-karl-storz-endoskope-ref-27002kp-pediatric-uretero-renoscope-7-3-fr-non-sterile-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27002KP, Pediatric Uretero-Renoscope 7.3 Fr., NON STERILE, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1054-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27010L, Uretero-Renoscope, 7 Fr., 43cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1055-2025-karl-storz-endoskope-ref-27010l-uretero-renoscope-7-fr-43cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27010L, Uretero-Renoscope, 7 Fr., 43cm, NON STERILE, RxONLY, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1055-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1056-2025-karl-storz-endoskope-ref-27000l-uretero-renoscope-7-fr-6-43-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1056-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27001L, Uretero-Renoscope, 8 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1057-2025-karl-storz-endoskope-ref-27001l-uretero-renoscope-8-fr-6-43-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27001L, Uretero-Renoscope, 8 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1057-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27011L, Uretero-Renoscope, 8 Fr., 6¿, 43cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1058-2025-karl-storz-endoskope-ref-27011l-uretero-renoscope-8-fr-6-43cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27011L, Uretero-Renoscope, 8 Fr., 6¿, 43cm, NON STERILE, RxONLY, CE ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1058-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27002L, Uretero-Renoscope, 9.5 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1059-2025-karl-storz-endoskope-ref-27002l-uretero-renoscope-9-5-fr-6-43-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27002L, Uretero-Renoscope, 9.5 Fr., 6¿, 43 cm, NON STERILE, RxONLY, ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1059-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27010K, Ureteroscope, 7 Fr., 34 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1060-2025-karl-storz-endoskope-ref-27010k-ureteroscope-7-fr-34-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27010K, Ureteroscope, 7 Fr., 34 cm, NON STERILE, RxONLY, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1060-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27000K, Ureteroscope, 7 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1061-2025-karl-storz-endoskope-ref-27000k-ureteroscope-7-fr-6-34-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27000K, Ureteroscope, 7 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1061-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27001K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1062-2025-karl-storz-endoskope-ref-27001k-ureteroscope-9-5-fr-6-34-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27001K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1062-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27002K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123](https://isitonrecall.com/recall/fda-device-z-1063-2025-karl-storz-endoskope-ref-27002k-ureteroscope-9-5-fr-6-34-cm-non-sterile-rxonly-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27002K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1063-2025%22) Dec 19, 2024 FDA device enforcement ### [KARL STORZ - ENDOSKOPE, REF: 27011K, Ureteroscope, 8 Fr., 6¿, 34cm, CE 0123](https://isitonrecall.com/recall/fda-device-z-1064-2025-karl-storz-endoskope-ref-27011k-ureteroscope-8-fr-6-34cm-ce-0123/) Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for KARL STORZ - ENDOSKOPE, REF: 27011K, Ureteroscope, 8 Fr., 6¿, 34cm, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1064-2025%22) Oct 21, 2024 FDA device enforcement ### [Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC](https://isitonrecall.com/recall/fda-device-z-0363-2025-irrigation-tubing-for-karl-storz-endomat-select-up210-ref-031523-10-tubing-set-irrigation-pc/) Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CO, CT, DC, MD, MI, MN, NC, NY, OH, OK, TN, TX, WA. [Official source for Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0363-2025%22) Oct 11, 2024 FDA device enforcement ### [4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5 x 120 mm REF 28205NDS Aggr. Pro Line Shaver Blade, steril...](https://isitonrecall.com/recall/fda-device-z-0526-2025-4-5-x-180-mm-ref-28208bks-aggressive-cutter-sterile-6x-3-5-x-70-mm-ref-28206cbs-full-radius-resector/) Due to holes detected in the inner barrier system that may compromise the sterility of the affected products. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AL, FL, IA, IN, KS, MA, MO, MT, NJ, NY, OH, PA, TX, TN, and VA. The countries of Canada and Germany. [Official source for 4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Res...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0526-2025%22) Jul 23, 2024 FDA device enforcement ### [Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123](https://isitonrecall.com/recall/fda-device-z-3218-2024-karl-storz-endoskope-ref-27092ama-hopkins-telescope-6-rx-only-ce-0123/) Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ,... [Official source for Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3218-2024%22) Jul 23, 2024 FDA device enforcement ### [Karl Storz - Endoskope , REF: 27093AA Hopkins Telescope 6, Rx only, CE 0123](https://isitonrecall.com/recall/fda-device-z-3219-2024-karl-storz-endoskope-ref-27093aa-hopkins-telescope-6-rx-only-ce-0123/) Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ,... [Official source for Karl Storz - Endoskope , REF: 27093AA Hopkins Telescope 6, Rx only, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3219-2024%22) ## Reasons in these listed records - Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact the assurance of sterility. - Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance. - Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. - Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S. These examples come from this result page and are not a ranking of every recall reason. ## Checking Karl Storz Endoscopy ### Is there a recall on karl storz endoscopy right now? This archive contains 52 records, including 52 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 Karl Storz Endoscopy](https://isitonrecall.com/check/?q=Karl%20Storz%20Endoscopy) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)