Defective Shoulder Replacement Device Recalled; High Fracture Rate
On behalf of the Larry Wall Trial Law posted on February 27, 2017
Defective Shoulder Device RecalledFDA RECALLS SHOULDER DEVICE According to a U.S. Food & Drug Administration report, on February 16, 2017, Zimmer Biomet recalled its Comprehensive Reverse Shoulder System Humeral Tray Model 115340 because the defective devices are fracturing at a higher rate than stated in the labeling. The device fracture are resulting in revision surgeries Read More
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