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Masimo Corporation recalls Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9895 Rx Only,
Recalled April 24, 2024 · FDA recall Z-1539-2024 · Masimo
Hazard
Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring. · FDA Class II
Units
65
Sold at
Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, FL, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY and the countries of Algeria, Argentina, Australia, Austria, Bahrain, Belgium, Belize, Bolivia, Burkina Faso, Burundi, Cambodia, Canada, Chile, Colombia, Congo, The Democratic Republic of, Costa Rica, Cyprus, Czech Republic, Ethiopia, Finland, France, Germany, Greece, Guatemala, Hong Kong, India, Indonesia, Israel, Italy, Japan, Lesotho, Mozambique, Netherlands, New Zealand, Nigeria, Norway, Oman, Pakistan, Panama, Poland, Puerto Rico, Qatar, Rwanda, Saudi Arabia, Senegal, Singapore, Slovakia, Slovenia, Spain, Sweden, Switzerland, Tanzania, United Republic Of, Thailand, Trinidad And Tobago, Uganda, United Kingdom, Uruguay, Yemen, Zimbabwe.
Description
Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.
Product
Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9895 Rx Only,
Manufacturer(s)
Masimo Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →