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FDA Warns Consumers to Avoid TimeOut Capsules

FDA Warns Consumers to Avoid TimeOut Capsules

The U.S. Food and Drug Administration is warning consumers not to take TimeOut Capsules because it contains an active drug ingredient that can dangerously lower blood pressure. The product is marketed as a dietary supplement for sexual enhancement.
U.S. Food And Drug Administration Issues Miracle Mineral Solution Warning

U.S. Food And Drug Administration Issues Miracle Mineral Solution Warning

The U.S. Food and Drug Administration is warning consumers not to take Miracle Mineral Solution, an oral liquid also known as “Miracle Mineral Supplement” or “MMS.”  The product, when used as directed, produces an industrial bleach that can cause...
Two EpiPen Doses Recommended for Severe Food Allergies

Two EpiPen Doses Recommended for Severe Food Allergies

ChildrensHospital.org – In a large six-year review of emergency department (ED) data, researchers at Children’s Hospital Boston, in collaboration with Massachusetts General Hospital, found that many children with severe food-related allergic...
ETHEX Corporation Recalls Specific Lots of 30 Mg. And 60 Mg. Morphine Sulfate Extended Release Tablets

ETHEX Corporation Recalls Specific Lots of 30 Mg. And 60 Mg. Morphine Sulfate Extended Release Tablets

ETHEX Corporation announced today that it has voluntarily recalled specific additional lots of morphine sulfate 60 mg extended release tablets, and specific lots of morphine sulfate 30 mg extended release tablets, as a precaution, due to the possible...
ETHEX Corporation Voluntarily Recalls a Single Lot of Morphine Sulfate 60 Mg Extended Release Tablets

ETHEX Corporation Voluntarily Recalls a Single Lot of Morphine Sulfate 60 Mg Extended Release Tablets

ETHEX Corporation announced today that it has voluntarily recalled a single lot of morphine sulfate 60 mg extended release tablets (Lot No. 91762) due to a report of a tablet with twice the appropriate thickness.
Actavis Totowa (formerly Known As Amide Pharmaceutical, Inc.) Recalls All Lots of Bertek And UDL Laboratories Digitek® (digoxin Tablets, USP)

Actavis Totowa (formerly Known As Amide Pharmaceutical, Inc.) Recalls All Lots of Bertek And UDL Laboratories Digitek® (digoxin Tablets, USP)

Actavis Totowa LLC, a United States manufacturing division of the international generic pharmaceutical company Actavis Group, is initiating a Class I nationwide recall of Digitek® (digoxin tablets, USP, all strengths) for oral use.
Denture Cleansers: Allergic Reactions And Misuse

Denture Cleansers: Allergic Reactions And Misuse

FDA has received at least 73 reports of adverse reactions, including at least one death, related to the use of denture cleansers. Problems have occurred with both proper and improper use of these products.
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