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From: U.S. Food & Drug Administration (FDA) <fda@service.govdelivery.com>
Date: Tue, Jul 29, 2014 at 3:29 PM
Subject: Hospira Announces Voluntary Nationwide Recall Of One Lot Of Lidocaine HCI Injection, USP, 2 percent, 20 mg per mL Single-dose Vial, Preservative-free, Due To Particulate Matter
To: iammejtm@gmail.com
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From: U.S. Food & Drug Administration (FDA) <fda@service.govdelivery.com>
Date: Tue, Jul 29, 2014 at 3:29 PM
Subject: Hospira Announces Voluntary Nationwide Recall Of One Lot Of Lidocaine HCI Injection, USP, 2 percent, 20 mg per mL Single-dose Vial, Preservative-free, Due To Particulate Matter
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.
07/29/2014 03:39 PM EDT
Hospira, Inc. (NYSE: HSP), announced today it will initiate a voluntary recall of one lot of Lidocaine HCI Injection, USP, 2 percent, 20 mg per mL, 5 mL single-Dose Vial, Preservative-Free (NDC 0409-2066-05; Lot 25-550-DD, Expiry 1JAN2015) to the user level due to a confirmed customer report of discolored product with visible particles in the solution as well as particulate embedded in the molded glass container. Hospira has identified the particulate as iron oxide. To date, Hospira has not received reports of any adverse events associated with this issue for this lot.
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Jeremy Tobias Matthews
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