GE Healthcare, LLC recalls Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

Recalled July 19, 2017 · FDA recall Z-2703-2017 · GE Healthcare

Hazard

Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and Unexpected System Malfunction · FDA Class II

Units

3,448 (334 US; 3,114 OUS)

Sold at

US Distribution including PR and to the states of : AL, AR, AZ, CA, CO, CT, FL GA, ID,IL, IN, KY, LA, , MA, MD, MI, MO, MS, MT, MN, NC, NH, NJ, NV, NY, OH, OK, PA, TN, TX, VA, WA, WI, and UT. OUS: Algeria Argentina Australia Austria Belgium Bolivia Bosnia and Herzegovina Brazil Bulgaria Cambodia Canada Chile Colombia Costa Rica Cote d'Ivoire Croatia Czech Republic Ecuador Egypt El Salvador Estonia Finland France Germany Greece Honduras Hong Kong Hungary India Indonesia Iraq Ireland Israel Italy Japan Jordan Kenya Korea (Republic Of) Kuwait Latvia Lebanon Lithuania Malaysia Maldives Malta Mauritius Mexico Moldova Morocco Myanmar Netherlands New Zealand Nigeria Norway Oman Pakistan Paraguay Peru Philippines Poland Portugal Romania Russia Saudi Arabia Senegal Serbia Singapore Slovakia Slovenia South Africa Spain Sweden Switzerland Taiwan Tanzania Thailand Turkey United Arab Emirates United Kingdom Uruguay Vietnam Zimbabwe

Description

Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and Unexpected System Malfunction

Product

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

Manufacturer(s)

GE Healthcare, LLC

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