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FDA Designates Four Class I Recalls In Four Days

This article was originally published in The Gray Sheet

Executive Summary

FDA announced a spate of class I recalls between May 20 and May 23, for Maquet Datascope’s intra-aortic balloon pumps, CareFusion’s Alaris Pump Module infusion pump software, Baxter’s ABACUS total parenteral nutrition calculation software, and Fisher and Paykel Healthcare’s infant nasal CPAP prongs.

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