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Nihon Kohden America Inc recalls WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/ 008419831
Recalled March 10, 2021 · FDA recall Z-1162-2021 · Nihon Kohden America
Hazard
Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter. · FDA Class II
Units
4,436
Sold at
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.
Description
Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Product
WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/ 00841983102561 ORG 9700A/No UDI
Manufacturer(s)
Nihon Kohden America Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →