Stryker Oasys Spine Device Recall One in a Stream of Issues
Device Maker Stream of Issues. Undergoing spinal surgery is a frightening and worrisome prospect for patients, and patients agree to these typically complex procedures believing the medical device products being used in their surgeries—and in their bodies—are safe and effective. In the case of the Stryker Orthopedics’ Oasys … [Read more...] about Stryker Oasys Spine Device Recall One in a Stream of Issues
Class I recall issued on PEEK Ardis Inserter device used in spinal surgery; sales of accompanying system halted
Federal health regulators have issued their most serious warning about a medical device used during spinal surgery, the PEEK Ardis Inserter. According to a statement from the Food and Drug Administration, the agency has deemed a callback on the Zimmer PEEK Ardis Inserter device a Class I recall. The manufacturer had previously … [Read more...] about Class I recall issued on PEEK Ardis Inserter device used in spinal surgery; sales of accompanying system halted
