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Esbelder Man, Fem and Siloutte Capsules Vitamin Supplements Recalled due to Undeclared Ingredients 26 Aug 2013 | 03:09 pm
The FDA informs consumers and health professionals that the Esbelder Man, Fem and Siloutte Capsules are recalled because they contain undeclared Sibutramine, N-Desmethylsibutramine, and N-di-Desmethyl...
Aidapak Services Select Repackaged Pharmaceuticals Recalled due to Potential Incorrect Labeling 23 Aug 2013 | 03:06 pm
Pharmacy personnel, health professionals and patients are informed by the FDA that Aidapak Services Select Repackaged Pharmaceuticals are recalled due to potential incorrect labeling that may cause se...
Fluoroquinolone Antibacterial Drugs: Risk for Possibly Permanent Nerve Damage 22 Aug 2013 | 03:07 pm
The FDA informs infectious disease, family practice and pharmacy professionals that the labels of Fluoroquinolone Antibacterial drugs are updated to better describe the serious adverse event of periph...
Hospira Blood Sets Recalled (Class I) due to Instances of Outer Wall of Blood Bags Punctured with Piercing Pin 21 Aug 2013 | 03:14 pm
Health professionals and risk managers are informed by the FDA that certain Hospira Blood Sets are recalled due to instances of outer wall of blood bags punctured with piercing pin that may cause seri...
MRidium 3860+ Infusion Systems equipped with MRidium 1145 Dose Error Reduction System (DERS) Drug Library Kit Recalled (Class I) due to Potential for ... 20 Aug 2013 | 02:55 pm
The FDA informs Biomedical Engineering, Radiology, Nursing, and Risk Managers that the MRidium 3860+ Infusion Systems equipped with MRidium 1145 Dose Error Reduction System (DERS) Drug Library Kit is ...
Optease Retrievable Inferior Vena Cava (IVC) Filter Recalled due to Labeling Correction 19 Aug 2013 | 03:19 pm
Risk Managers, cardiology and surgery personnel are informed by the FDA that the Optease Retrievable Inferior Vena Cava (IVC) Filter is recalled due to labeling correction to prevent implanting the fi...
Tranquility Recalled due to Undeclared Drug Ingredient 16 Aug 2013 | 02:05 pm
The FDA informs the consumers that quantity lots of Tranquility are recalled because they contain Doxepin and Chlorpormazine. Background of Tranquility Tranquility, by Health and Beyond LLC, is used ...
CareFusion Alaris PC Unit (Model 8015) with version 9.12 Keyboard Processor Recalled (Class I) due to Potential Loss of Communication between Componen... 15 Aug 2013 | 03:20 pm
Biomedical Engineer personnel and Risk Managers are informed by the FDA that the Alaris PC Unit (Model 8015) with version 9.12 Keyboard Processor is recalled due to potential loss of communication bet...
Best Slim 40 Pills Recalled due to Undeclared Ingredients 14 Aug 2013 | 03:18 pm
The FDA informs health professionals, consumers and patients that Best Slim 40 pills are recalled because they contain the ingredient Sibutramine that may pose significant threat to patients. Backgro...
Bethel Advance and Quick Thin Recalled due to Undeclared Ingredients 13 Aug 2013 | 03:22 pm
Health professionals, consumers and patients are informed by the FDA that Bethel Advance and Quick Thin are recalled because they contain undeclared Sibutramine and Phenolphthalein that may pose serio...
