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FDA Issues Class I Recall of Zimmer Biomet’s Comprehensive Reverse Shoulder Device

On February 16, 2017, the FDA issued a Class I recall of Zimmer Biomet’s Reverse Shoulder Humeral Tray, which is the most serious type of recall due to the potential for severe injury. The Comprehensive Reverse Shoulder is a surgically implanted shoulder replacement device that is intended to help restore arm movement in patients with …. Read More

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