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Dobutamine Hydrochloride Injection Lawsuit


Labeling Errors Prompts Recall of 250 mg/20 ml Injections


Incorrect Dosages Prompt Recall of Dobutamine Hydrochloride Injection

Incorrect Labeling States Dosage at 1000 times above Indicated

Certain lots of Dobutamine Hydrochloride Injection 250 mg/20 ml are being recalled due to a labeling error which indicates units of measure for dosing 1000 times higher than recommended.

The recall has been issued by Novopharm Ltd., in consultation with Health Canada. So far, 3 lots of this product are being recalled. They are: Lot 957734 (expiry date: June 30, 2009), Lot 957735 (expiry date: September 30, 2009) and Lot 1156284 (expiry date: April 30, 2010).

Dobutamine hydrochloride is indicated in the treatment of adults with cardiac decompensation due to depressed contractility resulting from organic heart disease or following cardiac surgical procedures in which parenteral therapy is necessary for inotropic support.

JAN-12-09: Recall of certain lots of Dobutamine Hydrochloride Injection [HEALTH CANADA: DOBUTAMINE HYDROCHLORIDE RECALL]

Legal Help

If you or a loved one has suffered adverse health effects or damages as a result of receiving this product at an incorrect dosage, please click the link below and your complaint will be sent to a lawyer who may evaluate your claim at no cost or obligation.
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