Masimo Corporation recalls Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, Rx Only,

Recalled April 24, 2024 · FDA recall Z-1538-2024 · Masimo

Hazard

Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring. · FDA Class II

Units

4978 units

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:9849, Rx Only,

Manufacturer(s)

Masimo Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →