Sendx Medical Recalls
2 recalls on record · September 5, 2012 to November 14, 2012 · Medical Devices
November 14, 2012Medical DevicesFDA
Sendx Medical Inc recalls ABL80 FLEX CO-OX analyzer, model #393-841 (all software versions prior to 1.35). The ABL80 FLEX CO-OX is a portable,
Hazard: The recall was initiated because SenDx Medical Inc. became aware of a software issue in the ABL80 FLEX CO-OX analyzer related to the reporting of the hemoglobin fractional parameters.
September 5, 2012Medical DevicesFDA
Sendx Medical Inc recalls ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) - pH Blood Gas and Electrolytes Analyzer Syst
Hazard: The firm recalled because the glucose measurements from a patient sample that the customer felt was too low and did not reflect the patient's clinical condition.