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The articles on our Web site include some of the publications and papers authored by our attorneys, both before and after they joined our firm. The content of these articles should not be taken as legal advice or as an expression of the views of the firm, its attorneys or any of its clients. We hope the articles spur discussion in the legal community with insight into the experience of the authors. We expressly reserve the right in the future to become wiser or simply change our mind.



Mass Tort Articles

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May 4, 2009

Consumer Alert: Hydroxycut Recalled

On May 1, 2009, the U.S. Food and Drug Administration (FDA) warned consumers to immediately stop using the diet drug Hydroxycut.
February 19, 2009

Consumer Alert: ETHEX and KV Pharmaceutical Recall

On January 26, 2009, KV Pharmaceutical announced the voluntary recall of most of its products, in addition to the voluntary suspension of nearly all of its manufacture and shipping processes.
February 4, 2009

Consumer Alert: FDA Reports Recall of the BioSense Webster LASSO 2515 Variable Circular Mapping Catheter

On September 3, 2008, the FDA issued an Enforcement Report that included a Class II Recall of the BioSense Webster LASSO 2515 Variable Circular Mapping Catheter.
January 30, 2009

Chantix Patients Report Dangerous Side-Effects

The drug Chantix, sold by Pfizer to patients trying to quit smoking, has been associated with serious psychiatric side effects and even suicide.
August 13, 2008 Attorney-Client Privilege and the In-House Counsel

Attorney-Client Privilege and the In-House Counsel

Los Angeles Daily Journal
The role of in-house counsel has increasingly expanded to encompass participation in decisions about business, technical, scientific, public relations and advertising issues, in addition to purely legal issues. This dual role can raise significant complications during discovery.
June 13, 2008

Update: Increased Concern over Mounting Numbers of Reported Deaths and Serious Injuries Prompt the FDA to Order Testing of Medical Devices Containing Heparin

The FDA has found an association between a conaminant in the blood-thinning drug heparin and servere adverse reactions which are being reported.
May 21, 2008

Consumer Alert: Digitek Heart Failure Medications Recalled - A Serious Risk of Injury or Death to the Patient

On April 25, 2008 Actavis Totowa LLC (formerly known as Amide Pharmaceutical, Inc.) announced the Class I nationwide recall of all strengths of oral Digitek tablets, which is a brand name for digoxin tablets, USP 0.125 mg and 0.25 mg.
March 13, 2008

Update: FDA Finds Contaminant In Heparin, Which Is Being Investigated for Severe Allergic Reactions and Death

Last week, the FDA announced they have found an "unknown contaminant" in the blood-thinning drug heparin that is produced by Baxter HealthCare Corporation.
February 29, 2008

Consumer Alert: Baxter's Heparin Investigated for Severe Allergic Reactions and Death

Recently, serious adverse events have been reported in patients who received heparin manufactured by Baxter HealthCare Corporation.
February 15, 2008

Fentanyl Patches Recalled

On February 12, 2008, PriCara announced that patches containing the prescription painkiller “fentanyl” are being recalled.
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