January 26, 2010
FDA notified healthcare professionals of a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets, and Exel/Exelint "Securetouch+" Safety Huber Infusion Sets due to 'coring,' the cutting or dislodging of silicone cores or slivers from the ports into which they are inserted).
December 21, 2009
Procter & Gamble has announced a voluntary recall of its Vicks DayQuil Cold & Flu (acetaminophen, dextromethorphan HBr, phenylephrine) 24-count LiquiCaps Bonus Pack because the product does not contain a child-resistant backing for the blister packs in the box, despite label statements that it is in child-resistant packaging.
December 08, 2009
Bayer Consumer Care has issued a voluntary recall of one lot of the combination package of Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels.
November 20, 2009
The FDA and Procter & Gamble have notified consumers of a voluntary recall of Vicks Sinex UltraFine Mist Nasal Spray.
November 02, 2009
The FDA has sent a warning letter to Procter & Gamble notifying the company that its Vicks DayQuil Plus Vitamin C (acetaminophen, dextromethorphan HBr, phenylephrine HCl, vitamin C) and Vicks NyQuil Plus Vitamin C (acetaminophen, doxylamine succinate, dextromethorphan HBr, vitamin C) for the relief of cold and flu symptoms are illegally marketed.