The FDA is reminding healthcare professionals that oral nimodipine capsules should be given only by mouth or through a nasogastric tube and should never be given by intravenous administration.

Lundbeck announced a voluntary nationwide recall of two lots of NeoProfen (ibuprofen lysine) Injection that failed to meet a visible particulate quality requirement.

Nutraloid Labs and the FDA have announced a nationwide recall of some lots of Nutraloid Labs' ejaculoid XXTREME and stimuloid II, sold as dietary supplements.

The Prescribing Information for Afluria (trivalent, inactivated, "split virus" influenza vaccine [Types A and B], from CSL Biotherapies) has been updated to inform healthcare professionals of an increased incidence of fever and febrile seizure among young children in Australia, mainly those <5years of age.

The FDA has warned consumers not to use Miracle Mineral Solution, an oral liquid also known as "Miracle Mineral Supplement" or "MMS."

The FDA has notified healthcare professionals and patients that it is reviewing reports of adverse effects from Evamist (estradiol transdermal spray, from Ther-Rx) in children who may have been unintentionally exposed to the drug through skin contact with women using this product.

The FDA has notified healthcare professionals and patients about the potential for developing eosinophilic pneumonia while receiving the antibiotic Cubicin (daptomycin, from Cubist).

The FDA is warning healthcare professionals not to use unapproved intrauterine devices (IUDs).

The FDA is warning consumers that Joyful Slim herb supplement, marketed as a natural herb for weight loss, contains undeclared desmethyl sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss.

Good Health announced a voluntary recall of Vialipro, sold as a dietary supplement, after FDA lab analyses found certain batches of the product to contain undeclared sulfoaildenafil.