Thursday, June 26, 2008

U.S. Food & Drug Administration (FDA) Daily Digest Bulletin

Update : 1

From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Wed, 25 Jun 2008 07:48:04 -0500 (CDT)
Subject: Oncology Drugs Update: Velcade (bortezomib) is Approved for Initial Treatment of Patients with Multiple Myeloma

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Center for Drug Evaluation and Research, U.S. Food and Drug Administration
HHS Logo links to Department of Health and Human Services website

Velcade (bortezomib) is approved for initial treatment of patients with multiple myeloma.
More information: http://www.fda.gov/cder/offices/oodp/whatsnew/bortezomib2008.htm


Update : 2
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Wed, 25 Jun 2008 07:52:04 -0500 (CDT)
Subject: CDRH New Update

Skip NavigationFDA Logo links to FDA home pageCenter for Devices and Radiological Health, U.S. Food and Drug AdministrationHHS Logo links to Department of Health and Human Services website

FDA Home Page | CDRH Home Page | Search | A-Z Index U.S. Food and Drug AdministrationCenter for Devices and Radiological Health Questions?
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CDRHNEW Logo Date: June 25, 2008

The following new items were added to the CDRH web pages on June 24, 2008. Previous CDRH New Items can be found on the CDRHNew Page.

* Federal Register: Medical Devices; Change of Name; Technical Amendment. Text PDF

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Update : 3
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Wed, 25 Jun 2008 08:02:44 -0500 (CDT)
Subject: Recall of Nestle Pure Life Purified Water (June 24)

Recall of Nestle Pure Life Purified Water (June 24)
Wed, 25 Jun 2008 07:23:00 -0500

This announces a product recall for the one-gallon Nestle Pure Life Purified Drinking Water sold ONLY in Shop-Rite stores in the five Northeast states of Connecticut, Delaware, New Jersey, New York and Pennsylvania. This affects ONLY the one-gallon size.


Update : 4
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Wed, 25 Jun 2008 08:19:18 -0500 (CDT)
Subject: FDA Warning Letters Update

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