Archive for March, 2011

FDA Announces the Approval of Iron Dextran for Baby Pigs

The Food and Drug Administration (FDA) announced today the approval of Uniferon (injectable iron), for the prevention and treatment of iron deficiency anemia in baby pigs.

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Identifying Recalled Products

Think you may have a recalled product? Watch this video to learn who to contact and how to identify an unsafe product by the numbers and dates on the packaging.

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X-Hero and Male Enhancer: Recall – Undeclared Drug Ingredient

Products marketed as dietary supplement contain drug ingredients sulfosildenafil or tadalafil, which may interact with

nitrates found in some prescription drugs and lower blood pressure to dangerous levels.

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Roche ACCU-CHEK FlexLink Plus Infusion Set: Class I Recall – Potential for Under-Delivery of Insulin

Use of recalled product can result in elevated blood glucose levels (hyperglycemia), which can lead to serious health complications including death.

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Soladek Vitamin Solution: Unapproved Product May Contain Dangerously High Levels of Vitamins A and D

Reports of consumers experiencing decreased renal function, elevated levels of calcium in the blood, fatigue, heart arrhythmia, vomiting, and diarrhea.

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Featured

USA Far Ocean Group Inc. Issues Voluntary Nationwide Recall of X-Hero and Male Enhancer, Products Marketed as Dietary Supplements

X-Hero and Male Enhancer Dietary Supplements

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Featured

Recall of Arnica Flower And Stem Arnica Due To Inaccurate Usage Information On Product Label

NAC Foods Corporation of Palisades Park, New Jersey is announcing a voluntary recall of the Mi Pepito Arnica Flower and Stem Arnica due to inaccurate usage information on the product label. The current label states ‘Use to enhance the flavor of your favorite dish.’

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Bad Reaction to Cosmetics? Tell FDA

Have you had a negative reaction to a hair dye or makeup, body wash or lotion? If you have, FDA’s office of cosmetics wants you to report it.

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Celerite Slimming Tea: Recall – Undeclared Drug Ingredient

Product marketed as a dietary supplement contains sibutramine, which may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

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Irinotecan Hydrochloride Injection: Recall – Fungal Microbial Contaminant

Non-sterility of a chemotherapeutic product administered via the intravenous route has the potential to result in infections which could be fatal, especially in patients who are immunocompromised.

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