Recall

J&J bought troubled Norian XR manufacturer to help own reputation

The Pennsylvania-based company Synthes produced a bone cement called Norian XR, which has been linked to the deaths of five patients who received it for spine surgery. Four high-ranking Synthes executives ended up doing jail time for their role in illegally marketing Norian, despite allegedly being aware of the health risks it presented.

Ironically, pharmaceutical giant Johnson & Johnson acquired Synthes specifically as a means of dealing with damage to J&J’s own reputation in the wake of what Fortune magazine describes ...

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J&J hopes to overcome troubles from recalls

Investment Website Seeking Alpha says that healthcare products giant Johnson & Johnson is poised to announce its third-quarter earnings report. The company is hoping to break a streak of revenue declines over the last two quarters, as well as net income declines over the past four quarters.

The report says Wall Street has a mixed view on the advisability of investing in the company. Goldman Sachs, for example, recently downgraded the ...

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Critics: EU medical device plan falls short

European Union officials are considering more stringent regulations for medical devices. But according to a report on MedPage Today, some European health advocates complain that the proposed regulations wouldn’t go far enough.

The report quotes Andrew Boulton, MD, president of the European Association for the Study of Diabetes, as saying: “We feel the proposals are a step in the right direction but we need many more steps to address patient safety.”

The ...

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Pharmacy linked to meningitis recalls all products

The New England Compounding Center, the Massachusetts pharmacy linked to a deadly outbreak of fungal meningitis, has voluntarily recalled all of its products.

The meningitis has been linked to a steroid medication injected into the spine to treat back pain. According to a story in the Chicago Tribune, the New England Compounding Center said there’s no indication that any other products have been contaminated and the recall is being undertaken purely as a precautionary measure.

The U.S. Food and Drug Administration had ...

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FDA warns hip implant manufacturer

According to a story posted on Fox News, the U.S. Food and Drug Administration has issued a warning letter to medical device maker Zimmer Holdings Inc., mentioning concerns about the manufacture of certain hip implants.

The letter was sent following an agency inspection of the company’s plant in Puerto Rico, which found manufacturing and testing issues related to the company’s Trilogy Acetabular System products — implanted in hip-replacement surgery.

The report came ...

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Researchers: Women shouldn’t get metal hip implants

Researchers in the U.K. have recommended that women not receive all-metal hip replacements because of the procedure’s early failure rate, Bloomberg reports.

In a study published in the Lancet medical journal, scientists who analyzed data from the National Joint Registry for England and Wales found that women experience more problems than men in the seven years after surgery. They also found that “metal-on-metal” resurfacing implants fail more quickly than total hip ...

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