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From: U.S. Food & Drug Administration (FDA) <fda@service.govdelivery.com>
Date: Fri, Jul 11, 2014 at 7:08 AM
Subject: Hospira Issues Voluntary Nationwide Recall Of One Lot Of Lactated Ringers And 5% Dextrose Injection, Usp, 1000 Ml, Flexible Containers Due To Mold Contamination
To: iammejtm@gmail.com
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From: U.S. Food & Drug Administration (FDA) <fda@service.govdelivery.com>
Date: Fri, Jul 11, 2014 at 7:08 AM
Subject: Hospira Issues Voluntary Nationwide Recall Of One Lot Of Lactated Ringers And 5% Dextrose Injection, Usp, 1000 Ml, Flexible Containers Due To Mold Contamination
To: iammejtm@gmail.com
You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).
This information has recently been updated and is now available.
07/11/2014 09:16 AM EDT
Hospira, Inc. (NYSE: HSP), announced today it is initiating a voluntary nationwide user-level recall of one lot of Lactated Ringers and 5% Dextrose Injection, USP, 1000 mL, Flexible Container, NDC 0409-7929-09, Lot 35-118-JT, Expiry 1NOV2015 . This action is due to one confirmed customer report where particulate was identified within the solution of the primary container.
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Jeremy Tobias Matthews
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