FDA warns J&J unit over device marketing

08/24/2010 | Los Angeles Times (tiered subscription model)

The FDA issued a warning letter to DePuy Orthopaedics saying that the Johnson & Johnson unit is selling an unapproved device, the TruMatch Personalized Solution System, and marketing another device, the Corail Hip System, for off-label uses. A DePuy statement said the company is "reviewing the letter to understand the FDA's concerns and will respond to their request for information."

View Full Article in:

Los Angeles Times (tiered subscription model)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Senior Director, Biostatistics
Edwards Lifesciences
Irvine, CA
Diagnostic Technician
Roche
Marlborough, MA
Test Technician
Roche
Marlborough, MA
Associate - Food and Drug
Keller and Heckman LLP
Washington, DC
Senior Paralegal - Research & Development, and Medical
Boehringer Ingelheim
Ridgefield, CT