Zimmer Initiates Class 2 Recall of Persona Trabecular Metal Tibial Plate

The Food and Drug Administration issued a press release from Zimmer, Inc., on March 12, 2015 “initiating a voluntary recall of Persona Trabecular Metal Tibial [plate] following an increase in complaints of radiolucent lines and loosening. All sizes and lots of the affected devices are being removed from distribution.” The company asks that any healthcare…

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Medical Devices Contain Antibiotic Resistant “Superbug” CRE

The Centers for Disease Control and Prevention call it the “nightmare bacteria.” It has been implicated in the deaths of hospital patients in both Los Angeles, California and in Seattle, Washington. It is also the basis for new lawsuits against medical device manufacturers. The “superbug” is Carbapenem-Resistant Enterobacteriaceae (CRE), bacteria which “kill up to half…

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