Zimmer Biomet Comprehensive Reverse Shoulder Recall
The Food & Drug Administration has issued a Class 1 recall on the Zimmer Biomet Comprehensive Reverse Shoulder. The FDA has noted that the device has a high fracture rate. A Class I recall is the most critical type of recall issued by the FDA. Those who continue to use devices that are the subject of a Class I recall may … [Read more...] about Zimmer Biomet Comprehensive Reverse Shoulder Recall
Zimmer Biomet Recalled with a Class I Designation Lawsuits
Zimmer Biomet just issued a recall on its Implantable Spinal Fusion Stimulators over the devices' potential to contaminate patients with harmful chemicals. The chemicals may be toxic due to the possibility of harmful chemicals that may be toxic to the body's tissues and organs, according to the U.S. Food and Drug Administration … [Read more...] about Zimmer Biomet Recalled with a Class I Designation Lawsuits
