Hospira continues to struggle with serious problems related to its GemStar Infusion System and its accessories. The latest bad news came Wednesday, when the FDA designated a recall of the GemStar Power Supply, 3VDC, as Class I.
It is the fifth time in nearly three years that FDA regulators thought an issue around a GemStar-related recall could result in serious injury or death, and it is the eighth time overall that Hospira has faced a Class I recall. (Only three other medical device companies—Johnson & Johnson, Medtronic, and General Electric—have had more Class I recalls than Hospira since the start of 2012.)
Help employers find you! Check out all the jobs and post your resume.
