Philips Respironics Esprit Ventilator Recall Is Class I
Philips' (NYSE:PHG) Respironics issued a recall for its Esprit V1000 and V200 ventilators over concerns that machines may fail to operate on AC power.
The FDA classified the action as a Class I recall, meaning that use of the device could result in serious injury or even death. The respirators are used to provide breathing assistance to adults and children, including newborns.
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The FDA classified the action as a Class I recall, meaning that use of the device could result in serious injury or even death. The respirators are used to provide breathing assistance to adults and children, including newborns.
Help employers find you! Check out all the jobs and post your resume.