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    Posted on May 7, 2014 To

    Taking an Aspirin a Day May Prevent Heart Attacks for Some, But Others Must be More Careful, FDA Warns

    The Food and Drug Administration (FDA) has warned that the general statement that “taking an aspirin a day” may help to prevent heart attacks may not be true for everyone, and it can even cause some dangerous side effects, according to its website. On Monday, the FDA announced that it would not be granting Bayer Corp. its requested approval of listing aspirin as one of the drugs known to combat heart attacks and strokes, according…

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    Posted on May 1, 2014 To

    After Warning, Johnson & Johnson Postpones Sale of Device Used for Fibroid Surgery

    Johnson & Johnson has temporarily suspended its international sale of its power morcellators following an April 17 advisory from the Food and Drug Administration warning that their use to remove fibroids from the uterus has a risk of worsening hidden cancer, according to Reuters. The company says that it will attempt to resume sale once their role in fibroid treatment is further investigated and understood by the medical community, Reuters reported. Laparoscopic power morcellation is…

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    Posted on April 29, 2014 To

    Senators Request Department of Transportation to Force GM’s Hand

    Democratic Senators Edward Markey (MA) and Richard Blumenthal (CT) urged the Department of Transportation to take action to ensure that owners of the estimated 2.6 million recalled GM models to cease driving them until they are repaired, according to Reuters. The National Highway Traffic Safety Administration, who has been investigating the failure of GM to take action to combat the defects, has authority to pursue recalls of vehicles deemed as unsafe, but they cannot force…

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    Posted on March 17, 2014 To

    FDA Proposed New Food Labeling

    A proposal by the Food and Drug Administration (FDA) is expected to significantly revise nutrition labels for the first time in 20 years, according to a report by The Wall Street Journal (“Food Labels Set for New Look,” Feb. 27, 2014). In a story by Thomas M. Burton and Annie Gasparro, it was reported that the Obama administration is looking for food labels to have larger-font calorie counts and more realistic portion sizes so that…

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    Posted on March 14, 2014 To

    GM’s Massive Recall on Ignition Switches Triggers Federal Criminal Probe

    In response to criticism stemming from a failure to properly investigate complaints of ignition switch failures in many of their models, General Motors has hired a private investigator to determine if the company failed to adequately respond to the dangerous condition. The New York Times reported that over the last 11 years, GM has received more than 260 complaints of cars spontaneously shutting down while drivers were on highways, in city traffic, and even on…

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    Posted on February 4, 2014 To

    Possible Dangers and Complications with Testosterone-Boosting Drugs

    The Food and Drug Administration (FDA), a federal agency tasked with keeping the American public aware of potential health risks like E. Coli and pharmaceutical side effects, is warning that there could be a link between testosterone-boosting pills and increased risk of heart problems and fatalities. According to the Chicago Tribune, many men take these drugs due to the persuasive nature of the marketing efforts that coined the phrase “low-T” without fully researching the possible…

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    Posted on January 17, 2014 To

    Children Enjoy Their New Toys, But Are They Safe?

    Children remind us of the innocence and joy of the holidays year-round, which is why it is so important for parents today to monitor the toys their children play with to keep the kids safe. Product recalls are down by almost 66% over the past five years, but it is stringent safety mandates, dangerous toys being seized upon their import and vigilant parents that are responsible for this laudable trend. Most toys are not meant…

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    Posted on December 2, 2013 To

    Medtronic Heart Devices Being Recalled

    After four reports were filed about problems with the heart implant, the FDA mandated a recall due to possible injury and death possibilities. As reported by the AP, the problem is rooted in the occurrence of wear and the dislodging of materials that can block critical arteries. As of this time, no patient or recipient has died, but the forecasted complications could be fatal, according to the Wall Street Journal.

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    Posted on November 21, 2013 To

    FDA Moves to Close Loophole

    Back in 2011, the Pliva v. Mensing ruling from the Supreme Court of the United States revealed a loophole in federal regulation of generic drugs. Generic drug manufacturers were not responsible for the updating of labels; it was left to brand name companies. In the past two years, the Food and Drug Administration (FDA) has moved towards closing this regulation loophole. After a public comment period, requirements are expected to change and these generic drug…

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