Link: http://www.digiteklawsuit.org/

A Digitek Recall Lawsuit has stemmed from a FDA class I recall of the drug Digitek. The Digitek Recall Lawsuit states that Actavis Totowa who manufactures Digitek did not comply with certain Federal Regulations and due to manufacturing errors, certain lots of the Digitek Recall Lawsuit tablets were produced containing twice the active ingredient Digoxin which can lead to severe medical complications such as seizures, cardiac instability, and even death. The Digitek Recall Lawsuit alleges that this Digitek manufacturing error would not have occurred if Actavis Totowa had reacted adequately to previous FDA warnings about meeting certain manufacturing safety standards where the Digitek Recall Lawsuit tablets were being produced.

Due to the serious medical conditions that could arise from Digitek toxcicity, the Digitek Recall Lawsuit plaintiffs are looking for compensation for their injuries as well as future health problems associated with taking the Digitek Recall Lawsuit tablets that were double dosed. If you are one of the many people who have taken Digitek and experienced certain adverse reactions, you may want to be part of the Digitek Recall Lawsuit. If you are looking for a Digitek Lawsuit lawyer, make sure your attorney has experience in working with medical malpractice cases. These types of cases go on for months on end, sometimes years before reaching any type of settlement. Make sure your lawyer involved in the Digitek lawsuit will fight for you. You want to have an open line of communication with your Digitek lawyer and know that they will communicate with you as the case progresses. Make sure you are comfortable in talking with your Digitek lawyer and that they have the legal expertise to guide you through the Digitek Recall Lawsuit.

Digitek is prescribed for people who have cardiac problems such as irregular heartbeat, artrial fibrillation, and congestive heart failure. The Digitek Recall Lawsuit was started because some of the Digitek tablets contained twice the regular dose due to a manufacturing error. Involved in the Digitek Recall Lawsuit are those that were prescribed these tablets and experienced certain severe medical complications from taking the Digitek Lawsuit double dosed tablets. There are many families who are taking part in the Digitek Recall Lawsuit because of the medical problems they now have associated with the recalled Digitek tablets. If you are one of these people who were prescribed Digitek, you may want to contact a Digitek Lawyer who is familiar with the Digitek Recall Lawsuit.

Our lawyers are here to help answer your questions about the Digitek Recall Lawsuit. If you are seeking answers or want more information about the Digitek class action lawsuit, fill out the provided webpage form and a Digitek Lawyer will contact you.

Link: http://www.digiteklawsuit.org/

In April of 2008 a letter was issued by Actavis Totowa issuing a voluntary recall of their drug Digitek. At the time of the Digitek recall, the FDA had already received several reports of illnesses and medical events related to Digitek treatment.
The Food & Drug Administration (FDA) deemed the Digitek recall a Class I recall, meaning that the defective Digitek tablets could cause serious health problems or death.

Digitek (Digoxin) is a drug is used to treat artrial fibrillation and heart rhythm disorders by helping the heart beat stronger and with a more regular rhythm. Digitek is available in tablet, capsule, liquid, and injectable forms, however the recall pertains only to the tablets. The reason for the Digitek recall was due to the possibility that some of the tablets contained twice the approved dosage. Medical providers have found that tablets subject to the Digitek recall, if ingested, can result in severe medical complications, generally caused by digitalis toxicity, which is a medical condition that can lead to very serious side effects, sometimes including death

A Digitek class action lawsuit was filed in US District Court in New Jersey after April's Digitek recall brought to light significant questions about how the defective pills were manufactured.How does this happen one might ask themselves and how can we foresee a “Digitek recall”. Would having a crystal ball help? Maybe, but in this case reading the warning letter Actavis Totowa received back in 2006 for failing to provide periodic safety reports at its facility where Digitek was manufactured would certainly give us some insight.

Because of the severe risk of Digitek toxicity associated with this manufacturing error, individuals who currently take or have taken the drug should consider developing a Digitek lawsuit. Some of these lawsuits allege that the Digitek recall would not have been necessary if Actavis Totowa had adequately responded to earlier warnings from the FDA about the quality of the Digitek being produced. Additional information about the recall can also be found at Digitek Recallwebsite.

The plaintiffs in the Digitek lawsuit are seeking compensation for their injuries as well as medical monitoring in case they experience future health problems. With a Digitek lawsuit, our lawyers may help you get reimbursed for expenses such as medical bills, loss of income, and pain and suffering.

We are pursuing individual litigation nationwide and currently accepting new Digitek recall and Digitalis toxicity cases in all 50 states.If you would like to discuss your legal rights or want more information on the Digitek recall lawsuit, our experienced lawyers would be happy to answer your questions. Click Digitek Attorney for a Digitek recall attorney consultation.

Link: http://www.digiteklawsuit.org/

The Digitek recall caused a lot of anxiety among pharmaceutical consumers, as the worst possible side effects included death. Many rumors swirled around the Digitek recall, making the story seem even more sensational than it is. Following is a discussion of the true facts that led to the Digitek recall and information as to who qualifies for a class action lawsuit.

The Digitek recall happened in April, 2008, when the Digitek manufacturers realized that some of their pills contained nearly twice the intended level of their active ingredient, digoxin. Digitek was manufactured in New Jersey by UDL Laboratories, Inc. under the trade name “UDL” and by Mylan Pharmeceuticals under the trade name “Bertek.” A New Jersey company called Activis Totowa was responsible for both manufacturers which made the defective pills that caused the Digitek recall.

Digitalis toxicity, or digoxin poisoning, has a number of very serious side effects, including brachycardia, low blood pressure and death, which prompted the manufacturers to institute the Digitek recall.

The manufacturer that released the dangerous pills which led to the Digitek recall had received a warning from the FDA as far back as three years earlier that they needed to institute better quality control methods, according to an article on the online pharmaceutical journal In-Pharmatechnologist.com (Taylor, 2008)

If you took Digitek during 2005-2008 and experienced any of the following symptoms, you may qualify as a member of the class action lawsuit against the manufacturer who caused the Digitek recall: abnormally low urine output, cold sweats, difficulty breathing in a prone position, dizziness, excessive urge to urinate, fainting, heart palpitations, lack of appetite, lowered blood pressure, nausea and/or vomiting, unexplained death, uneven pulse, very slow heart rate, or vision changes.

To find out if you qualify for the class action which relates to the Digitek recall, search the words Digitek recall plus attorney, or Digitek recall plus class action. Alternately, you can look in a legal directory for lawyers who specialize in class actions in your state and contact them.

The class action lawsuit for the Digitek recall will seek to identify all people who received the faulty Digitek pills and suffered ill health as a result. Rather than suing individually, a class action is a more efficient method of identifying all victims of the Digitek recall and allowing one member to serve as a class representative. Each member of the class will get some monetary benefit as a result of the Digitek recall lawsuit if the plaintiffs’ attorneys win the case.

The intent of the Digitek recall lawsuit is to get monetary compensation for the victims, as well as provide incentive to pharmaceutical manufacturers to institute better quality control in order to avoid any further situations like the Digitek recall.

If you want to be a class member of the Digitek recall lawsuit, you’ll need to present an attorney with proof that you used the medicine in the time frame noted above. If you were using the medicine during this time, a pharmacist should have contacted you and notified you of the Digitek recall, and he or she should have records of this use.

To contact an attorney regarding a possible Digitek Recall Lawsuit, please see Digitek Recall.