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File:Hospira Issues A Voluntary Nationwide Recall of One Lot of Vancomycin Hydrochloride For Injection USP, Equivalent to 1 g Vancomycin (Sterile Powder) Due to Uncontrolled Storage During Transit (24103394022).jpg

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Description Hospira, Inc., a Pfizer company, has announced a voluntary recall of one lot of, MAGNESIUM SULFATE IN WATER FOR INJECTION (0.325 mEq Mg**/mL) 40 mg/mL 2g total, 50 mL (NDC: 0409-6729-24, Lot 53-113-JT, Expiry 1NOV2016) to the user level due to a confirmed customer report of an incorrect barcode on the primary bag labeling. The product has a barcode identifying the product contents on both the overwrap and on the primary container. The barcode on the overwrap is correct; however, there is potential for the primary container barcode to be mislabeled with the barcode for HEPARIN SODIUM 2000 USP UNITS/1000 mL in 0.9%SODIUM CHLORIDE INJECTION.
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Source Hospira Issues A Voluntary Nationwide Recall of One Lot of Vancomycin Hydrochloride For Injection USP, Equivalent to 1 g Vancomycin (Sterile Powder) Due to Uncontrolled Storage During Transit
Author The U.S. Food and Drug Administration

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Public domain
Unless otherwise noted, the contents of the Food and Drug Administration website (www.fda.gov) —both text and graphics— are public domain in the United States. [1] (August 18, 2005, last updated July 14, 2015)
This image was originally posted to Flickr by The U.S. Food and Drug Administration at https://flickr.com/photos/39736050@N02/24103394022. It was reviewed on 9 September 2016 by FlickreviewR and was confirmed to be licensed under the terms of the United States Government Work.

9 September 2016

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current05:43, 9 September 2016Thumbnail for version as of 05:43, 9 September 2016977 × 1,017 (38 KB)Vanished Account Byeznhpyxeuztibuo (talk | contribs)Transferred from Flickr via Flickr2Commons

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