FDA Recalls Posted August 25, 2025 Share Posted August 25, 2025 On August 22, 2025,the US FDA’s Center for Biologics Evaluation and Research has suspended the biologics license for Valneva Austria GmbH’s Ixchiq (Chikungunya Vaccine, Live). This vaccine was initially approved by FDA under the accelerated approval pathway in November of 2023 for the prevention of View the full article Quote Link to comment Share on other sites More sharing options...
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