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Home › FDA recalls J&J's orthopedic device because of fracture potential

 

FDA recalls J&J's orthopedic device because of fracture potential

2013-02-23 09:07:41| Biotech - Topix.net

The U.S. Food and Drug Administration on Friday said it has notified healthcare professionals of a Class I recall, the most serious type, of an orthopedic device made by Johnson & Johnson.

Tags: potential device recalls fda

Category:Biotechnology and Pharmaceuticals

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