| Class 2 Device Recall PSG1100 Sleep Diagnostic System. | |
Date Initiated by Firm | December 21, 2020 |
Date Posted | January 14, 2021 |
Recall Status1 |
Open3, Classified |
Recall Number | Z-0865-2021 |
Recall Event ID |
87011 |
510(K)Number | K120888 |
Product Classification |
Full-montage Standard Electroencephalograph - Product Code GWQ
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Product | 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. |
Code Information |
Serial numbers 3. Serial numbers 320, 470, 507, 534, 621, 757, 770, 795, 892, 1165-1183, 1186- 1205, 1214-1293, 1295-1297, 1304-1330, 1333-1342, 1358 -1384, 1387-1389, 1391-1413, 1421-1430, 1434-1505, 1507- 1516. |
Recalling Firm/ Manufacturer |
Nihon Kohden America Inc 90 Icon Foothill Ranch CA 92610-3000
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For Additional Information Contact | Nihon Kohden America Technical Services Group 800-325-0283 |
Manufacturer Reason for Recall | Medical device non-conformance to electrical safety standard (IEC 60601-1). |
FDA Determined Cause 2 | Device Design |
Action | On 12/21/2020, the firm , Nihon Kohden, sent out an "URGENT RECALL NOTIFICATION" letter dated 12/21/2020 to all affected consumers . The letter described the product, problem and actions to be taken. The customers were instructed to do the following:
1. Inform potential users in your organization of this notification.
2. Complete the attached reply form and return it to the fax number (949) 580-1550 or email it to: JB110@NKUSA.com or JB110@nihonkohden.com.
If you have any questions, please call the Toll-free: 1-800-325-0283, Option 6 (Monday-Friday,8am-5pm PDT) or E-mail: JB110@NKUSA.com or
JB110@nihonkohden.com. |
Quantity in Commerce | 189 Units |
Distribution | 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. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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510(K) Database | 510(K)s with Product Code = GWQ
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