Stryker Recalls Spine Device After Fracture Reports

Stryker is conducting a Class 1 recall of its OASYS Midline Occiput Plate after reports of fracture of the pin that connects the implant’s tulip head to the plate body. This issue could lead to serious adverse health consequences including blood loss, nerve injury and the need for revision surgery to replace the implant, according to an FDA notice.
The GMP Letter