Respironics Issues Ventilator Recall
Respironics Inc. recalled its Trilogy 100, 200, and 202 ventilators due to a potentially defective electronic component in the medical device that could fail and cut ventilation to the patient and, in some cases, do so without sounding a warning alarm. The Food and Drug Administration (FDA ) classified the Respironics ventilator recall as a Class I, the agency’s most serious