Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
WMTS Telemetry Receiver Recalled by Nihon Kohden America Inc Due to Incorrect Date Stamp or No Data Transfer on...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Nihon Kohden America Inc directly.
Affected Products
WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/ 00841983102561 ORG 9700A/No UDI
Quantity: 4,436
Why Was This Recalled?
Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Where Was This Sold?
This product was distributed to 46 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MS, MO, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, TN, TX, UT, VT, VA, WA, WV, WI, WY, DC
About Nihon Kohden America Inc
Nihon Kohden America Inc has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report