Nihon Kohden America Inc: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: July 9, 2014. Most recent: November 13, 2024.

Risk classification: Class II: 6

Most recent recalls

DateAgencyProduct
November 13, 2024FDAAdult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 an…Z-0314-2025
November 6, 2024FDANihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Dis…Z-0267-2025
November 6, 2024FDANihon Kohden Adult Ear Clip SpO2 Sensor, 1.5 meter Model 809030007 Reusable SpO2 Ear C…Z-0268-2025
June 12, 2024FDABSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside M…Z-2025-2024
April 19, 2017FDABedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The Problem only affec…Z-1768-2017
July 9, 2014FDACNS-6200 Series Central Nurse Station and accessories. Model Number: CNS-6201 For car…Z-1979-2014

Questions about this company

How many recalls does Nihon Kohden America Inc have?
Recalert has 6 U.S. recalls on record for Nihon Kohden America Inc, published between July 9, 2014 and November 13, 2024.
What was the most recent Nihon Kohden America Inc recall?
FDA recall Z-0314-2025, published November 13, 2024: 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 endoscopy type procedure…
Which agencies have handled Nihon Kohden America Inc recalls?
Nihon Kohden America Inc appears as the recalling firm in recalls from: FDA (6).

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