Stryker Craniomaxillofacial Division: Medical Device Recalls in 2013

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Stryker Craniomaxillofacial Division in 2013. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

2013

2015

Stryker Part Numbers 79-43903 (3cc), 79-43905 (5cc), 79-43910 (10 cc), 79-43915 (15cc), 397003 (3cc), 397005 (5cc), 397010 (10 cc), 397015 (15 cc) HydroSet Injectable HA Bone Substitute Sterile R/EO, nonpyrogenic, Product of Ireland Stryker Injectable Cement is a self-setting, calcium phosphate cement intended for use in the repair of neurosurgical burr holes, contiguous craniotomy cuts and other cranial defects as well as in the augmentation or restoration of bony contour in the craniofacial skeleton. The powder is mixed with the sodium phosphate/PVP solution provided in the kit and loaded into the empty cement delivery syringe to be applied directly to the site for void filling or augmentation.