Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate

Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate

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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Recalled Product:

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  1. Pingback: Zimmer Biomet Shoulder Recalled Due to High Fracture Rate – Daily Hornet | Breaking News That Stings!

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