Zimmer Biomet Issues Recall on Comprehensive Reverse Shoulder, Citing High Fracture Rate
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...]

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