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Baxter Initiates Voluntary Nationwide Recall Of One Lot Of Iv Solution Due To The Pot

Discussion in 'FDA Recalls' started by Food and Drug Administration, Jul 31, 2015.

  1. DEERFIELD, Ill., July 30, 2015 - Baxter International Inc. announced today it is voluntarily recalling one lot of intravenous (IV) solution to the hospital/user level due to the potential for leaking containers, particulate matter and missing port protectors. Baxter was made aware of these issues through customer complaints.

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