
According to Reuters, the problem is a failure to operate properly at extremely high glucose levels.
The report says no patient injuries related to the malfunction have been reported in the United States. The company said ...
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According to Reuters, the problem is a failure to operate properly at extremely high glucose levels.
The report says no patient injuries related to the malfunction have been reported in the United States. The company said ...
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“Manufacturing problems and recalls are not just embarrassing,” she writes, “but they are a worrisome sign that management has taken its eye off the ball in many key respects.”
Maller specifically mentions a recall that Johnson & Johnson initiated for its LPS Diaphyseal Sleeve, ...
continue reading...Categories: Drug and Medical Device Lawsuits, Product News and Recalls

But lawyers in a Chicago trial over injuries allegedly caused by the devices have produced a document that appears to contradict Ekdahl’s statement.
A Bloomberg story references a document from the Health Hazard/Risk Evaluation ...
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The new regulations will give manufacturers 90 days in which to file applications including the results of clinical trials and other “valid scientific evidence” showing that the devices are safe and effective. Manufacturers who fail to produce this evidence will be ...
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A statement from the company acknowledges “disappointments” from 2012, and resultant damage to the company’s public reputation.
Johnson & Johnson’s annual proxy statement says, in part: “We worked to address several reputational challenges and continue to strive toward regaining the reputational standings that we expect of ourselves and ...
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Buffett recently released his annual letter to shareholders of Berkshire Hathaway, and it shows that Berkshire had dropped its holdings of Johnson & Johnson stock to below $1 billion for the first time since the end of 2005.
The blog item notes that Johnson & Johnson has gone ...
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