BY PETER LOFTUS
Johnson & Johnson has recalled more than 157,000 surgical stapler devices and accessories used in hemorrhoids treatment procedures due to potential malfunctions that pose a serious safety risk.
J&J's Ethicon Endo-Surgery division also has stopped selling one of the products in the U.S. "as part of a business decision," the company said.
http://online.wsj.com/article/SB10001424052970204098704578080853291021898.html?mod=rss_Health
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