| Subject: | Recall of 20 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP |
| Category: | Food and Drug Administration (FDA)
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| Published: | Tue, 9 Dec 2008 - 02:00 pm |
| Hospira, Inc.is notifying healthcare professionals of a recall of one lot (lot number 65-620-FW, expiration date May 1, 2010, NDC 0409-7902-09) of 20 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP in 1000 mL flexible plastic containers. A small number of the containers may be incorrectly labeled with a bar code for 5% Dextrose Injection, USP (NDC 0409-7922-09). The incorrect bar code could lead to a medication error resulting in the wrong drug being... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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