FDA warns of a battery-depletion problem in some pacemakers

Early May, the U.S. Food and Drug Administration (FDA) released a warning about a battery-depletion problem in some Medtronic pacemakers. Although no recall was issued, the FDA warns patients who use certain models of Medtronic pacemakers to be watchful for signs of a low battery. How are some pacemakers malfunctioning? The batteries in some Medtronic…

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Thousands of Kids Injured Each Year from Infant Walkers

We’re all familiar with baby and infant walkers – those wheeled contraptions that let babies roll around using their legs before they’re able to walk. If you’re reading this, you probably used one yourself when you were little, or maybe one of your kids did. However, the authors of a recent study urge anyone that…

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Limbrel Capsules Linked to Potentially Deadly Health Problems

On December 5, 2017, the Federal Drug Administration (FDA) recommended that Limbrel capsules, intended for the treatment of osteoarthritis, be recalled. The FDA advisory concerning Limbrel, which is manufactured by Primus Pharmaceuticals, stated that the product has been connected to incidents of liver injury and other serious health issues. The agency recommended that consumers immediately…

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Which Automakers Saw the Biggest Recalls in 2017?

For many, 2016 was the Year of the Recall. Takata’s defective airbags accounted for much of that total, but almost every major automaker faced a recall that year. As of December 20th, however, 2017 had seen its fair share of recalls, too: 28,146,661 recalled vehicles, to be exact. It falls far short of the 52,985,779…

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Sorin Stöckert 3T Heater Cooler Devices are Endangering Heart Bypass Patients

The Centers for Disease Control and Prevention (CDC) is currently telling cardiologists and hospitals that heater-cooler devices used during heart surgery pose risk for serious medical complications. The dangers exist because many of these devices may have been contaminated in the manufacturing process. The risks include life-endangering infections, weight loss, fatigue, unexplained fever, aches, and…

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Ikea’s Failure to Meet Voluntary Safety Standards Resulted in the Largest Furniture Recall in US History

Ikea, the flat-pack furniture behemoth with a flimsy object in every home, announced the recall of 29 million chests and dressers in a deal with federal regulators. The recalled units do not conform to voluntary safety standards for furniture, which suggest that extended drawers can carry up to 50lbs of pressure before the unit begins…

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Ohio Dole Plant Will Be Center of Listeriosis Lawsuit

On January 21, Dole temporarily suspended operations at their Springfield plant. Six days later, the company issued a voluntary recall of all packaged products produced there. The next day, the US Food and Drug Administration confirmed the presence of the pathogen Listeria monocytogenes at the processing facility. The contamination resulted in a small but widespread…

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