Recall StatusOpen, Classified
Date Initiated2021-01-08
Product Quantity4,436
Reason for Recall
Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Firm Action
An URGENT RECALL NOTIFICATION was sent to the consignees via FedEx on 01/27/2021.
Recall Instructions
1. Please notify all individuals that need to be made aware of this issue/recall, and that the recall notification should be posted with the affected products.
2. Complete the attached form and return to Nihon Kohden America.
3. If adverse reactions or quality problems are experienced with the use of this product, please report to the FDAs MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.
" Online: www.f da.gov/medwatch/report.htm
" Mail: Download form www.fda.gov/medwatch/getforms.htm or call 1-800-332-1088 to request a report form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
4. If adverse reactions or quality problems are experienced with the use of this product, please report the event to Nihon Kohden Technical Support at: 1-800-325-0283 or email
[email protected].
Issue Resolution
Nihon Kohden America plans to release a new software version for the ORG-9100A / ORG 9110A.
The ORG-9700A has the same issues but has been discontinued by the manufacturer and is no longer supported. Please contact your Nihon Kohden America Account Executive.
Root Cause
Software design
Distribution Pattern
US - AL, AZ, AR, CA, CO, CT, DE, DC, FL, GA, HI, ID, IL, IN, IA, KS,KY, LA, ME, MA, MD, MI, MS, MS, MO, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA WI, WV and WY.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.