Articles for “FDA and EPA”

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CPSC Lists Voluntary Recalls

October 25, 2010 by Kathy Hedrick|FDA and EPA

The Consumer Product Safety Commission has published notice of the following voluntary recalls:

Revised FDA Import Alerts

October 22, 2010 by Kathy Hedrick|FDA and EPA

The Food and Drug Administration has posted revised versions of the following Import Alerts on the detention without physical examination of:

CPSC Announces Oct 27 Closed Compliance Meeting

October 22, 2010 by Karen Marzullo|FDA and EPA

The Consumer Product Safety Commission has announced a closed meeting on October 27, 2010, in which the staff will brief the Commission on various compliance matters.

CPSC Lists Voluntary Recall

October 21, 2010 by Kathy Hedrick|FDA and EPA

The Consumer Product Safety Commission has published notice of the following voluntary recall:

CPSC Announces Recall of 2 Million Graco Strollers

October 21, 2010 by Karen Marzullo|FDA and EPA

The Consumer Product Safety Commission announced that Graco is voluntarily recalling about 2 million Graco Quattro Tour and MetroLite strollers due to risks of entrapment and strangulation.

Revised FDA Import Alerts

October 20, 2010 by Kathy Hedrick|FDA and EPA

The Food and Drug Administration has posted revised versions of the following Import Alerts on the detention without physical examination of:

CPSC Lists Voluntary Recall

October 20, 2010 by Kathy Hedrick|FDA and EPA

The Consumer Product Safety Commission has published notice of the following voluntary recall:

Revised FDA Import Alerts

October 19, 2010 by Kathy Hedrick|FDA and EPA

The Food and Drug Administration has posted revised versions of the following Import Alerts on the detention without physical examination of:

CPSC Lists Voluntary Recall

October 19, 2010 by Kathy Hedrick|FDA and EPA

The Consumer Product Safety Commission has published notice of the following voluntary recall:

FDA Issues Warnings to Marketers of Unapproved ‘Chelation’ Products

October 18, 2010 by Marie Rapport|FDA and EPA

The Food and Drug Administration warned eight companies on October 14, 2010 that their over-the-counter (OTC) chelation products, some of which are marketed as dietary supplements, are unapproved drugs and devices, and that it is a violation of federal law to make unproven claims about these products.