Three quick notes:
1. The April 30 recall applies to polyethylene implants manufactured between December 2016 and January 2017, and distributed between December 2016 and February 2020.
2. During a routine bacterial endotoxin testing of polyethylene implants, three samples were found to exceed accepted standards for endotoxin levels during a six-week period.
3. Zimmer Biomet did not receive any complaints related to the issue, which could cause adverse local tissue reactions, critical pain or aches, and severe, systemic reactions.
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