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Monthly Archives: March 2013

Stryker Warned About Quality and Marketing Compliance problems

Orthopedic medical device maker Stryker Corp. has received a warning letter from the U.S. Food and Drug Administration (FDA) following a quality control inspection at its Michigan facility in November. The facility is in Portage, Michigan and is home to Stryker Corp’s instruments division, though there are no details about what was found. The letter…

Monthly Archives: March 2013

FDA Begins Guarding the Gate — Increase in Medical Device Monitoring

The medical device division of the FDA is acting more like a watchdog than a lapdog according to a new analysis. The Center for Devices and Radiological Health (CDRH) reportedly issued one-third more warning letters in 2011 for dangerous devices than it did in 2008. Since 2007 there has been a 250 percent increase in…

Monthly Archives: March 2013

Judge Brian Martinotti Runs an Orderly Court — First Stryker Rejuvenate/ABG II Case Conference

On February 20, 2013 Judge Brian Martinotti held the first case management conference in Bergen County New Jersey. Approximately 50 lawyers attended the conference including counsel for Stryker. Several matters were on the agenda and after all in attendance announced their appearance for the record judge Martinotti issued several rulings that will jumpstart this litigation….