FDA recall record

Nihon Kohden PSG-1100 Sleep Diagnostic System recall — FDA Z-0865-2021

Medical device non-conformance to electrical safety standard (IEC 60601-1).

Class IIclassification
Z-0865-2021official record ID
Feb 3, 2021report date

Recall record at a glance

Official recordZ-0865-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmNihon Kohden America Inc.
Report dateFeb 3, 2021
Recall initiation dateDec 21, 2020
Quantity189 Units
LocationFoothill Ranch, CA, United States

Official product description

PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI (01) 04931921108383; Made in Japan The PSG-1100 Sleep Diagnostic System is a digital PSG amplifier intended to record the electrical activity of the brain (EEG) and other bio-potential signals and to record physiological data required for sleep studies.

Why the product was recalled

Medical device non-conformance to electrical safety standard (IEC 60601-1).

Distribution information

US Nationwide Distribution - CA, CO, CT, FL, ID, IL, IN, MA, MD, MI, MO, NC, NM, NY, SC, TX, TN, UT, VA, VT and WA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.