Fresh Recalls

Nihon Kohden America recalls

Recall found. Nihon Kohden America is named in FDA Class II recall Z-0089-2027 covering Product Name. Hazard: Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds and the visualization of alarms. Identifying details: Lot Code: CNS-6201 (PU-621RA), SW versions: 01-03, 01-04, 01-05, 01-06, 02-10, 02-11, and 02-40. Status: Ongoing.

Models with recalls

Product Name (1)

All Nihon Kohden America recalls

FDA Class II · Medical device · October 14, 2026

Product Name recall — Nihon Kohden America LLC

Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds…

Official ID Z-0089-2027 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.