Procedure For Filing New Valsartan Recall Claims Through Short-Form Complaint To Be Discussed During Status Conference

The U.S. District Judge presiding over all federal Valsartan recall lawsuits is scheduled to meet with parties involved in the litigation tomorrow, at which time the Court is expected to review the status of a “short-form” complaint, designed to allow additional plaintiffs to more easily file new claims against the manufacturers of different versions of the recalled hypertension drug distributed in recent years with cancer-causing impurities.

There are currently about five dozen product liability lawsuits pending in the federal court system against various generic drug manufacturers and distributors, each raising similar claims that problems with the manufacturing process resulted in pills being contaminated with known human carcinogens, including N-nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA).

As individuals diagnosed with liver cancer, kidney cancer, stomach cancer and other gastrointestinal tract cancers continue to contact lawyers and review new valsartan claims, the size of the litigation is expected to grow rapidly in the coming months and year.

VALSARTAN LAWSUITS

Were you prescribed contaminated Valsartan drugs?

Side effects of recalled valsartan may increase the risk of cancer, due to an impurity discovered in certain generic versions of the hypertension drug.

Learn More SEE IF YOU QUALIFY FOR COMPENSATION

Given common questions of fact and law presented in complaints filed in various different U.S. District Courts nationwide, the U.S. Judicial Panel on Multidistrict Litigation (JPML) established coordinated pretrial proceedings in February 2019, which resulted in the transfer of cases pending throughout the federal court system to U.S. District Judge Robert B. Kugler in the District of New Jersey. The process is designed to reduce duplicative discovery, avoid conflicting pretrial schedules and serve the convenience of the parties, witnesses and the judicial system.

On July 8, plaintiffs and defendants filed a proposed agenda (PDF) for a status conference set for July 10, indicating that the parties will review the status of developing a short form complaint, plaintiff fact sheet and other procedural matters.

In complex product liability litigation, where a large number of individuals are pursuing claims involving the same or similar allegations, it is common for the Court to adopt a streamlined process for filing new claims, where plaintiffs are able to bring cases through a “short form” complaint, which adopts more detailed allegations outlined in one single “master” complaint approved by the Court. The process is also designed to help standardize the gathering of information about a large number of cases, categorizing claims by injuries or allegations.

At a recent status conference, plaintiffs’ attorneys informed the court that they anticipate more than 2,000 valsartan recall claims will eventually will be filed on behalf of individuals nationwide.

As part of the coordinated pretrial proceedings, it is expected that Judge Kugler will establish a “bellwether” process where a representative group claims will be prepared for early trial dates in the MDL, to help the parties gauge how juries may respond to evidence and testimony that will be repeated throughout the litigation, and promote potential valsartan settlements with the manufacturers and distributors of the contaminated pills.

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits
Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits (Posted yesterday)

A federal judge has agreed to divide lawsuits over gastroparesis injuries linked to drugs like Ozempic and Mounjaro into multiple phases, examining how the condition is diagnosed and whether plaintiffs' claims are preempted by federal laws.

Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn
Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn (Posted 2 days ago)

Lawsuit alleges that Abbott Laboratories failed to provide families and the medical community with adequate warnings about the risks associated with it’s cow’s milk-based Similac formula, which a now adult woman indicates has left her with life-long NEC injuries.

Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects
Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects (Posted 3 days ago)

Six breast cancer patients have asked a federal judge for permission to amend a complaint filed in March 2024, which describes problems linked to the device and painful side effects experienced when the tissue marker migrated out of position or shattered inside their bodies.