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Nonin Medical, Inc recalls 8500M Handheld Pulse Oximeter
Recalled April 5, 2017 · FDA recall Z-1690-2017 · Nonin Medical
Hazard
Nonin manufactures and sells two 8500 handheld pulse oximeters (Model 8500 with no memory feature and the 8500M which has a memory feature). Some of the devices distributed may not have the correct pulse oximetry board with the integrated memory feature. · FDA Class II
Units
15 (11 US; 4 OUS)
Sold at
Distribution in US (MI, NC, OH, NC, VA), and CANADA
Description
Nonin manufactures and sells two 8500 handheld pulse oximeters (Model 8500 with no memory feature and the 8500M which has a memory feature). Some of the devices distributed may not have the correct pulse oximetry board with the integrated memory feature.
Product
8500M Handheld Pulse Oximeter
Manufacturer(s)
Nonin Medical, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →