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More Articles:

1. National Brands Inc. Issues a Nationwide Recall of Topaz brand ...
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. ...

2. FDA News Release - FDA Approves Drug for Patients with Advanced ...
FDA Approves Drug for Patients with Advanced Prostate Cancer. The U.S. Food and Drug Administration recently approved the injectable drug degarelix, the first new drug in several years for prostate cancer. Degarelix is intended to treat ...

3. Firm Recall/State Recall
Stryker's Craniomaxillofacial (CMF) business unit announced today that the US Food and Drug Administration (FDA) concluded on Dec. 18, 2008 that its recall of the following Stryker CMF's Custom Cranial Implant Kits is a Class I recall, ...

4. FDA Announces Class I Recall of Ophthalmic Surgical Device
FDA Announces Class I Recall of Ophthalmic Surgical Device. The U.S. Food and Drug Administration announced a Class I recall of lot no. UD30654 of Healon D, an ophthalmic viscosurgical device (OVD) manufactured by Advanced Medical ...

5. How did the Food and Drug Administration let Chinese melamine into ...
The deepening severity of the problem stands in sharp contrast to the continued insouciance of the Food and Drug Administration. When Canada voiced concern over milk-powder imports from the United States in late September, an FDA...

6. FDA Requires Warnings about Risk of Suicidal Thoughts and Behavior ...
Acting under the authorities of the Food and Drug Administration Amendments Act of 2007 (FDAAA), the FDA is requiring manufacturers of antiepileptic drugs to submit to the agency new labeling within 30 days, or provide a reason why they ...

7. do you know.The Food and Drug Administration (FDA) today warned ...
darlin12009 asked: what in the heck is going on? when will it end, i just received the 2nd notice today from the fda The Food and Drug Administration (FDA)

8. Video: Allergan Announces U.S. Food and Drug Administration (FDA...
New Prescription Product Increases Length Thickness and Darkness of E... ...IRVINE Calif. Dec. 26 /- Allergan Inc. (NYSE... ...,Video:,Allergan,Announces,US,Food,and,Drug,Administration,(FDA),Approval,of,Latisse(TM),--,First,and,Only ...

9. MultiVu Video Feed: U.S Food and Drug Administration (Fda...
First and Only Treatment Approved by the Fda For Hypotrichosis of... The US Food and Drug Administration (FDA) has approved LATISSE(T... Available only through a doctor LATISSE(TM) is a once-daily presc... LATISSE(TM) will be available ...

10. Allergan Announces U.S. Food and Drug Administration (FDA...
New Prescription Product Increases Length, Thickness and Darkness of Eyelashes.