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Joint Replacements

FDA Class I Recall: Zimmer Biomet Comprehensive Reverse Shoulder Implant

Zimmer Biomet Comprehensive Shoulder Replacement

February 15, 2017, the FDA announced a Class I recall of the Zimmer Biomet Comprehensive Reverse Shoulder implant because these devices are fracturing at a higher rate than stated in the labeling. If this occurs, patients may need a revision surgery to remove or replace the device.

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