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With 12 recalls in less than 36 months, Johnson & Johnson tops the list of the five medical devicemakers with the most Class I recalls between 2012 and the present, according to FDA data. Read More
Jury members in an ongoing bellwether trial over Johnson & Johnson’s Pinnacle hip system will be allowed to consider testimony from an expert who said the company should have known the product was unsafe, a judge ruled recently, landing a blow to the defense. Read More
With 12 recalls in less than 36 months, Johnson & Johnson tops the list of the five medical devicemakers with the most Class I recalls between 2012 and the present, according to FDA data. Read More
With 12 recalls in less than 36 months, Johnson & Johnson tops the list of the five medical devicemakers with the most Class I recalls between 2012 and the present, according to FDA data. Read More
Two years after the FDA proposed using device registries as tool to strengthen postmarket surveillance, some healthcare groups are saying the agency has not done enough to make that happen. Read More
This past spring, officials at the Saudi Food and Drug Authority destroyed millions of dollars’ worth of expired medical devices that were seized at ports, as part of a government effort to ensure products entering the country are valid and safe. Read More
Manufacturers of medical devices that contain nanomaterials should use a phased approach to evaluate risk to avoid unnecessary testing, an expert committee of the European Commission recommends. Read More