FDA Alerts Archive - September 2013
September 3, 2013
September 5, 2013
September 8, 2013
- Altaire Pharmaceuticals Carboxymethylcellulose Sodium 0.5 Percent Ophthalmic Solution Sold Under Wal-Mart, CVS, and Target Brands: Recall - Preservative May Not Be Effective Through Expiry
- University Compounding Pharmacy Injection Products: Recall - Lack of Sterility Assurance
- MOTRIN Infants Drops Original Berry Flavor 1/2 fl oz: Recall - Particles Identified
September 9, 2013
September 10, 2013
September 12, 2013
September 13, 2013
- Creafuse Powder Grape and Creafuse Powder Fruit Punch: Recall - Contains DMAA
- Bupivacaine HCL Injection 0.25% (2.5 MG/ML) and Bupivacaine HCL 0.75% (7.5 MG/ML), 30 ML Single-Dose Vials by Hospira, Inc.: Recall- Presence of Particulate Matter
September 17, 2013
- Shou Fu Ti Tun Guo Xiang Xing Jian Fei Jiao Nang: Public Notification - Undeclared Drug Ingredient
- HeartSine Technologies Samaritan 300/300P PAD Public Access Defibrillators: Recall - Power, Battery Issues
September 20, 2013
September 23, 2013
September 24, 2013
- Xzen 1200, Xzen Gold and Xzen XPress: Public Notification - Undeclared Ingredients
- XZone Premium: Public Notification - Undeclared Drug Ingredient
- Wood-E: Public Notification - Undeclared Drug Ingredient
September 25, 2013
- W.S. Badger Company Daily SPF 30 Kids & Baby Sunscreen Lotion: Recall - Microbial Contamination
- Arzerra (ofatumumab) and Rituxan (rituximab): Drug Safety Communication - New Boxed Warning, Recommendations to Decrease Risk of Hepatitis B Reactivation
September 27, 2013
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