May 31, 2017 | Today’s News
Today's Top Story FDA announces recall of Zimmer Biomet SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulators. The U.S. Food and Drug Administration (FDA) has announced a Class I recall of Zimmer Biomet SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulators due to higher than allowed levels of potentially cytotoxic chemicals found during routine monitoring procedures. The stimulators are implanted into the patient's back during spinal fusion procedures, and provide constant electrical stimulation to [...]