The U.S. Attorney's Office says an eastern Washington doctor pled guilty to augmenting recalled medical devices to sell them ...
The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback