The following is a listing of recent U.S. Food and Drug Administration (FDA) updates and activities:

• Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PE‐PUR Foam Debris: FDA Safety Communication

• Important Information for Blood Establishments and Transfusion Services Regarding Bacterial Contamination of Platelets for Transfusion 

• Four Lots of Quinapril Tablets by Lupin Pharmaceuticals: …

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