FDA Early Alert: Intersurgical Inc. Removes 22 mm Smoothbore breathing tubes and systems

FDA Early Alert: Arrow International Removes Products Containing Spring Wire Guide Components

FDA: Convenience Kit Correction: Cardinal Health Updates Use Instructions for Presource Packs Containing BD Alaris Pump Infusion Sets

FDA Requires Safety Labeling Changes for Glucagon-Like Peptide-1 Receptor Agonists (GLP-1Ras) Due to Potential Increased Risk But Serious Eye Conditions: FDA Safety Communication

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