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Hospira receives FDA warning letter

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LAKE FOREST, ILL. (Aug. 31, 2:05 p.m. ET) — Pharmaceutical and medical device company Hospira Inc. has received a warning letter from the Food and Drug Administration because the audible alarms on some of the infusion pumps made at its plant in La Aurora de Heredia, Costa Rica, are still experiencing problems despite manufacturing changes made to the pumps after their initial recall 18 months ago.

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