| Subject: | Voluntary Recall of Ketorolac Tromethamine Injection |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 21 Oct 2009 - 02:00 pm |
| The Food and Drug Administration (FDA) and American Regent are notifying healthcare professionals of a voluntary recall of all lots of Ketorolac Tromethamine Injection, USP 30 mg/mL, including NDC# 0517-0801-25 [30 mg/mL 1mL Single Dose Vial] and NDC# 0517-0902-25 [30 mg/mL 2mL Single Dose Vial (60 mg/2mL)]. Particulate matter in conjunction with crystallization is potentially present in the product, which may result in adverse events such as obstruction of blood vessels which can induce... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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