Think the FDA tests products it approves? Think again.

Hundreds of products and drugs get approved by the U.S. Food & Drug Administration every year. Many people mistakenly believe that the FDA, because it has approved a device or drug, has also tested the product before allowing the sale. But this is not the case: the FDA conducts no independent testing, but rather relies…

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Frequently asked questions about the Fiat Chrysler (Jeep) recall

If you drive a Jeep Grand Cherokee or Commander, chances are you’ve probably heard or paid close attention to the news regarding the defects in certain vehicles. We’ll try to answer a few questions you may have here. How do I know if my vehicle is part of these recalls? Find your vehicle’s vehicle identification number…

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Fredericksburg Traumatic Brain Injury Attorneys

Our firm handles cases throughout the City of Fredericksburg, Stafford County, Spotsylvania County, and surrounding areas.   After fighting for our client for many years, we recovered $3.25 million in a Fredericksburg premises liability case for a young child who suffered a traumatic brain injury as an infant.  We represented a Stafford County client in…

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Zofran and Birth Defects

  Zofran was developed to help cancer patients who were experiencing nausea and vomiting.  The FDA approved Zofran in 1998.  It was originally indicated for chemotherapy-induced nausea and vomiting, and was also approved to treat nausea and vomiting associated with radiation therapy, anesthesia, and surgery. Zofran was never approved for use in pregnant women to…

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Jules Bianchi’s Traumatic Brain Injury – Diffuse Axonal Injury

The family of French Formula One driver, Jules Bianchi, released a statement saying that Bianchi sufferred a serious traumatic brain injury in his crash at the Japanese Grand Prix.  The statement says that Bianchi suffered diffuse axonal injury and is in critical condition.  Bianchi is in the Intensive Care Unity of the Mie General Medical…

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FDA recalls NuVision drugs due to unsafe conditions, again

FDA recalls NuVision compounding pharmacy drugs over sterility concerns Following a July safety inspection of the Downing Lab’s  (aka NuVision Pharmacy) compounding pharmacy in Dallas, Texas, the FDA has issued a drug safety alert and a formal request to Downing Lab to immediately recall all of their drugs marketed as sterile.  This is the second…

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DePuy Synthes Craniomaxillofacial Distraction System: Class I Recall

Class I recalls of medical devices or drugs are the most serious type of recall. They are issued when there exists “a reasonable probability that use of these products will cause serious adverse health consequences or death,” according to the U. S. Food and Drug Administration. The FDA notified healthcare professionals on 8/28/2014 of a…

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