Hospira Inc.: Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq
Recall reason: Failed pH Specifications: Confirmed high out of specification (OOS) results for pH.. Recalled by Hospira Inc.. Distribution: Nationwide, Puerto Rico, United Arab Emirates, Israel, Kuwait, Bahrain, and Trinidad & Tobago. Classification (Class III — minor violation). Affected lots/NDC/dates: Lot #: 42-335-DK, Exp 1JUN2016; 48-128-DK, 48-129-DK, 48-261-DK, 48-262-DK, 48-351-DK, Exp 1DEC2016; 52-361-DK, Exp 1APR. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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