Another Recall For Spacelabs Healthcare's Arkon Anesthesia System

The FDA slaps Spacelabs Healthcare with a Class I recall of its Arkon anesthesia system due to a software bug. The FDA slapped Spacelabs Healthcare with a Class I recall after the medical device company pulled 16 of is Arkon anesthesia delivery devices due to a software bug. The recall, of the Arkon device equipped with version 2.0 software, involves devices sold to hospitals in North Carolina and South Carolina, according to the FDA. The Class I recall status denotes a problem that could cause serious injury or death.

Help employers find you! Check out all the jobs and post your resume.