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FDA Announces Class I Recall of Certain Infusion Set Needles
Huber needles used in implanted ports to withdraw blood, inject medications, and other solutions
The U.S. Food and Drug Administration today announced a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation.
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Product recall : amiodarone hydrochloride batches
All remaining stock of certain batches of amiodarone hydrochloride concentrate for solution for injection or infusion 50mg/ml is being recalled, following a class 3 medicines recall issued by the Medicines and Healthcare products Regulatory Agency.
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FDA Warns Consumers about Counterfeit Alli
The counterfeit products contain controlled substance sibutramine
The U.S. Food and Drug Administration is today warning consumers about a counterfeit and potentially harmful version of Alli 60 mg capsules (120 count refill kit).
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Safety of paracetamol use in patients taking warfarin should be seriously considered
The safety of paracetamol use among patients on warfarin should be given more serious consideration, according to the authors of a recent study that provides further evidence of a serious interaction between the two drugs (European Journal of Clinical Pharmacology2010;66:97).
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