Every recall we track for Radiometer America Inc — 6 in all — plus the complaints and injury reports the public filed about them.
Radiometer recalls ABL90 FLEX Analyzers with specific software versions due to security vulnerabilities that may cause shutdowns or reboots, risking delayed medical treatment.
Radiometer recalls ABL800 analyzers (models 393-800 and 393-801) due to software causing patient demographic and test result mismatches. Affected units include specific configurations with creatinin.
Radiometer recalls ABL800 FLEX with Crea models (ABL817, ABL827, ABL837) due to potential underestimation of creatinine levels, which may lead to kidney issues in patients undergoing radiocontrast x-rays.
Radiometer recalls ABL90 FLEX analyzers with software versions 3.3MR1 or below due to potential incorrect test results from aspirating Cal 2 solution instead of rinse solution during specific use patterns.
Radiometer recalls ABL800 blood analyzers with FLEXQ module that may display incorrect patient results due to barcode misinterpretation. Affected units have specific serial numbers.
