FDA Warns Consumers Not to Eat California Prime Produce and Orange ... - FDA.gov

FDA Warns Consumers Not to Eat California Prime Produce and Orange ... FDA.gov The FDA visited Orca as part of its audit checks to follow up on Setton Pistachio's recall. The FDA found that products subject to Setton Pistachio's recall had been repacked and distributed by Orca under the California Prime Produce and Orange County ...

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ZOLL Receives Clearance to Market New R Series BLS and R Series Plus Defibrillators
ZOLL Medical Corporation (Nasdaq GS: ZOLL), a manufacturer of resuscitation devices and related software solutions, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market and sell the new ZOLL R Series ® BLS and R Series Plus defibrillators.

FDA delays approval of Botox to treat spasticity - Reuters

Examiner.com
FDA delays approval of Botox to treat spasticity
Reuters
Allergan said the FDA indicated it must first review the company's proposed Risk Evaluation and Mitigation Strategy for the medicine before approving it for the movement disorder common to stroke sufferers. Botox and a competing drug also derived from ...
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Canadian Health Officials, Echoing the FDA, Determine Infant ... - Wall Street Journal

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Canadian Health Officials, Echoing the FDA, Determine Infant ...
Wall Street Journal - 4 hours ago
Earlier this week, controversy arose in the US when the FDA said tests showed that a few infant formula products available in the US contained traces of ...
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FDA Releases Details on Pet Food Recall - Food Safety News

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NexMed Files Investigational New Drug Application with FDA for Cancer Drug ... - MarketWatch (press release)

NexMed Files Investigational New Drug Application with FDA for Cancer Drug ...
MarketWatch (press release)
The FDA has 30 days to comment on the IND before NexMed can proceed with human testing. PrevOnco (the anti-ulcer compound, lansoprazole, approved under the ...
NexMed Files IND Application With FDA

ebertchicago: RT @GreatDismal: RT @SJ_Edwards:http://bit.ly/8YT32b FDA ... - Tweet Soup

ebertchicago: RT @GreatDismal: RT @SJ_Edwards:http://bit.ly/8YT32b FDA ...
Tweet Soup
The given text will be posted to twitter.com. You can use !url, !url-alias, !tinyurl, !title and !user as replacement text. This question is for testing ...

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FDA will review angiotensin-receptor blockers (ARBs) for cancer risk - MedCity News

The Star-Ledger - NJ.com
FDA will review angiotensin-receptor blockers (ARBs) for cancer risk
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The Food and Drug Administration (FDA) has joined the ranks of public health agencies reviewing a popular class of blood pressure medicines and its possible ...
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And the Emmy for"Autism Television" Goes to... - San Francisco Chronicle (blog)

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Poor treatment for common vertebral compression fractures
The advice and treatment given to patients with vertebral compression fractures is not satisfactory.

Pfizer gets FDA approval for intravenous Revatio - The Associated Press

Pfizer gets FDA approval for intravenous Revatio
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NEW YORK — Drug developer Pfizer Inc. said Friday the Food and Drug Administration approved an intravenous version of its high blood pressure drug Revatio. ...
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