A federal judge ordered a New Jersey company that sold injectable skin whitening and other beauty products to stop selling and recall some of its products because they are unapproved new drugs that may be unsafe, putting consumers at risk. U.S. District Judge Peter G. Sheridan entered a consent decree of permanent injunction today…
FDA Takes Action Against 500+ Websites Selling Unapproved Prescriptions
Genentech Recalls 3 Lots of Activase Due to Cracked/Leaking Vials
Genentech issues voluntary nationwide recall of three lots of Activase® (alteplase)-100 mg due to lack of sterility assurance of the sterile water for injection. Genentech, a member of the Roche Group, is voluntarily recalling three lots of Activase® (alteplase) 100mg vials, that were co-packaged with Sterile Water for Injection, to the hospital level. The vials of…
FDA Advises Against Use of Foshan’s Alcohol Pads or Antiseptic Towelettes
FDA alerts health care professionals and patients not to use alcohol pads or benzalkonium chloride antiseptic towelettes manufactured by Foshan Flying Medical Products. The U.S. Food and Drug Administration is alerting health care professionals and patients not to use alcohol pads or benzalkonium chloride antiseptic towelettes made by Foshan Flying Medical Products Co. Ltd., located…
Oxytocin Compounded with Lactated Ringers/Dextrose Recalled Due to Low Potency
Anti-Itch Lotion Recalled Due to Incorrect Active Ingredient
Glass Found in Injectable, Hospira Recalls Lot
Recall: Potential B. Cepacia Contamination in Mid Valley Cough Syrup
Mid Valley Pharmaceutical LLC issues voluntary recall of Doctor Manzanilla Cough & Cold and Doctor Manzanilla Allergy & Decongestant Relief syrup due to potential contamination with Burkholderia cepacia. Mid Valley Pharmaceutical is recalling lot# 23221701 of Doctor Manzanilla Cough & Cold and lot# 23221701 of Doctor Manzanilla Allergy & Decongestant Relief syrup to the consumer…
