Stryker Instruments Div. of Stryker Corporation: Medical Device Recalls in 2017

According to to data from the FDA, there were 2 medical device recalls made by Stryker Instruments Div. of Stryker Corporation in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• Stryker SmartLife Large Aseptic Housing (7126-120-000)
• Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a PROFESS Patient Tracker, and a PROFESS Adaptor Cable.