US FDA Classifies Recall of Teleflex's Inflatable Devices as 'Most Serious'

2024-06-09T130905Z_1184509058_RC2O78ACCNS7_RTRMADP_3_LILLY-ALZHEIMERS
June 13 (Reuters) – The U.S. Food and Drug Administration classified a recall of Teleflex’s TFX.N inflatable devices that increase blood supply to the heart muscle as “most serious.”

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