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Table of Contents
"Dear Doctor" Letters
Other Safety Notifications
HHS News Papers
Enforcement
Report Ind.
Recalls, Alerts,
Warnings
Report a Drug Reaction
MedWatch
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This page contains "Dear Doctor" letters, and other safety
information on products regulated by the FDA Center for Veterinary
Medicine (CVM) and other FDA components.
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"Dear Doctor" Letters
Letters issued to veterinary medicine professionals by
drug manufacturers alerting the professionals to important
safety information.
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ProHeart®6,
Sept. 13, 2004 | pdf |
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Deramaxx,
Novartis Animal Health US, December 22, 2003
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ProHeart®6,
Fort Dodge Animal Health, June 19, 2003 | pdf
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ProHeart®6, Fort Dodge
Animal Health, July 22, 2002 | pdf
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Baytril®, Bayer Corporation,
July 6, 2000 | pdf |
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EtoGesic®, Tablets,
Fort Dodge Animal Health, May 23, 2000 | pdf
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RIMADYLŪ, Pfizer, Inc., March 9, 2000
| pdf |
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Other Safety Notifications
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Questions and Answers Regarding the FDA Recall of ProHeart®6
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Docket No. 2004D-0160, CVM 200433. Guidance for Industry:
Use of unapproved hormone implants in veal calves. Page
18594 [FR Doc. 04-08075] April 8, 2004 [TXT]
PDF]
Comments due April 8, 2005
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Recall
-- Firm Press Release - Voluntary Recall of Petcurean GO!
NATURAL Pet Food Consumers Asked to Return Product to Store,
October 22, 2003
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Nationwide
Recall of Miracle Leg Paint Veterinary Drug Because of Potential
Health Risk to Animals and Humans, May 30, 2002
CVM Updates
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Alert to Pet Owners
- Recall of Petcurean Go! Natural Pet Food, November
3, 2003
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Environmental Warning
Added to Animal Euthanasia Products, July 22, 2003
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Contaminated Animal
Feed Supplements Recalled, March 22, 2002
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FDA Prohibits Nitrofuran
Drug Use in Food-Producing Animals, February 7, 2002
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Update on Illegal Compounding
of Clenbuterol Veterinary Drug Products, January 10,
2002
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Guidance Available on Dioxin In Animal Feed,
October 19, 1999
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Canadians Issue Warning About Dog Treats,
September 30, 1999
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HHS News Releases/Talk Papers
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FDA Talk Paper - Fort Dodge to Comply with FDA's Request to Recall ProHeart6 Injectable Heartworm Product from the Market Due to Serious Health Concerns, September 3, 2004
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FDA Statement - Statement on Dairy Cattle Deaths in Washington State, June 21, 2004
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FDA News -
FDA Responds to the Use of Illegal Hormone Implants in
Veal Calves , April
2, 2004
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FDA Statement - Pet
Turtles Pose Risk of Salmonella Infection for Infants
and Small Children, December 15, 2003
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Nationwide
Recall of Medalist Brand Pig Ear Pet Treats Due to Possible
Salmonella Contamination, revised May 26, 2000
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FDA
Alerts Health Professionals and Consumers to Nationwide
Recall of Clinipad Antiseptic Sterile Products, March
10, 2000
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FDA
Issues Nationwide Public Health Advisory About Contaminated
Pet Chews, October 1, 1999
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All
Egg and Egg-Containing Products from Belgium, France and
the Netherlands and Animal Feed from European Countries
to be Detained at Ports of Entry, June 11, 1999
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FDA
Stops Importation and Distribution of Contaminated Animal
Drugs, March 12, 1999
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FDA Enforcement
Report Index (Recalls and Legal Actions)
The FDA Enforcement Report is published weekly by the Food
and Drug Administration, U.S. Public Health Service, Department
of Health and Human Services. It contains information on
actions taken in connection with agency regulatory activities,
including all FDA-classified recalls.
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FDA's
Product Recalls, Alerts, and Warnings
Recalls are actions taken by a firm to remove a product
from the market. Recalls may be conducted on a firm's own
initiative, by FDA request, or by FDA order under statutory
authority.
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How to Report an Adverse
Drug Reaction
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MedWatch
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Recalls.gov
To provide better service in alerting the American people
to unsafe, hazardous or defective products, six federal
agencies with vastly different jurisdictions have joined
together to create www.recalls.gov -- a "one stop shop"
for U.S. Government recalls.
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EPA,
Counterfeit Pesticide Products for Dogs and Cats
Web page updated by mdt,
October 28, 2004, 9:30 AM ET
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