Stryker Corporation Recalls Spine Surgery Device, Tagged With FDA’s “Deadly” Label

free biotech news Get the latest biotech news where you want it. Sign up for the free GenePool newsletter today!

Stryker, a well known artificial hip and medical device manufacturer, is recalling devices used in spinal surgeries. The FDA has assigned its most serious warning label to the problem, indicating that using the device could result in serious injury or death. Stryker is already under fire over lawsuits involving its Stryker Rejuvenate and ABG II artificial hips, amid allegations of early failure of the devices and the risk of metallosis.

Help employers find you! Check out all the jobs and post your resume.

MORE ON THIS TOPIC