--- title: "Nihon Kohden America Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Nihon Kohden America Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/nihon-kohden-america-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Nihon Kohden America Inc recall records **4** reported ongoing 4 records in this archive. Latest source date Sep 18, 2024. 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 Sep 18, 2024 FDA device enforcement ### [Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 Forehead Probe, Adult, 10/Box](https://isitonrecall.com/recall/fda-device-z-0267-2025-nihon-kohden-adult-pediatric-forehead-disposable-spo2-sensor-0-9m-model-809030006-disp-spo2-forehead/) Due to oximeters not having FDA market approval or clearance to distribute in the U.S. Class II Reported ongoing Distribution: U.S.: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, KS, MA, MD, MI, MO, MT, NC, ND, NE, NH, OK, PA, SC, TX, VT, WA, and WI. O.U.S.: N/A [Official source for Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 For...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0267-2025%22) Sep 18, 2024 FDA device enforcement ### [Nihon Kohden Adult Ear Clip SpO2 Sensor, 1.5 meter Model 809030007 Reusable SpO2 Ear Clip, each](https://isitonrecall.com/recall/fda-device-z-0268-2025-nihon-kohden-adult-ear-clip-spo2-sensor-1-5-meter-model-809030007-reusable-spo2-ear-clip-each/) Due to oximeters not having FDA market approval or clearance to distribute in the U.S. Class II Reported ongoing Distribution: U.S.: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, KS, MA, MD, MI, MO, MT, NC, ND, NE, NH, OK, PA, SC, TX, VT, WA, and WI. O.U.S.: N/A [Official source for Nihon Kohden Adult Ear Clip SpO2 Sensor, 1.5 meter Model 809030007 Reusable SpO2 Ear Clip, each](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0268-2025%22) Apr 29, 2024 FDA device enforcement ### [BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside Monitoring System is intended to monitor, display and record physiological data to provide c...](https://isitonrecall.com/recall/fda-device-z-2025-2024-bsm-3000-series-bedside-monitor-ref-bsm-3572a-the-life-scope-bsm-3000-series-bedside-monitoring-syst/) Due to software issue the device may give false "SpO2 Probe Failure" alarm Class II Reported ongoing Distribution: U.S. Nationwide distribution in the state of IA. [Official source for BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside Monitoring S...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2025-2024%22) Apr 29, 2022 FDA device enforcement ### [Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administer supplemental oxygen, for patients who can wear a 20mm bite block, during endos...](https://isitonrecall.com/recall/fda-device-z-0314-2025-adult-cap-one-biteblock-ref-yg-227t-the-cap-one-biteblock-is-intended-to-sample-co2-and-administer-s/) Due to products being shipped/distributed to customers after the products expiration date had past. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CA, GA, ID, KY, MA, MO, NC, OR, and UT. [Official source for Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administe...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0314-2025%22) ## Reasons in these listed records - Due to oximeters not having FDA market approval or clearance to distribute in the U.S. - Due to software issue the device may give false "SpO2 Probe Failure" alarm - Due to products being shipped/distributed to customers after the products expiration date had past. These examples come from this result page and are not a ranking of every recall reason. ## Checking Nihon Kohden America Inc ### Is there a recall on nihon kohden america inc right now? This archive contains 4 records, including 4 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 Nihon Kohden America Inc](https://isitonrecall.com/check/?q=Nihon%20Kohden%20America%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)