Digitek recall

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[edit] Senators Question Competence of FDA Inspectors | InjuryBoard West ...

20 November 2008, by unknown The Little Falls, New Jersey plant where Digitek was manufactured by Actavis Totowa now stands empty after the massive Digitek recall in April of 2008, and a subsequent investigation that noted irregularities in the manufacture of more ...

[edit] Senators Question Competence of FDA Inspectors - InjuryBoard.com

20 November 2008, by

[edit] Following Digitek, Other Drug Recalls, Feds Seek to Shutter ... - Newsinferno.com

18 November 2008, by

[edit] Following Recalls, Digitek Manufacturer to Remain Shut Down - AboutLawsuits.com

17 November 2008, by

[edit] Digitek Manufacturer Actavis May be Forced to Close Sub-Standard ... - InjuryBoard.com

15 November 2008, by

[edit] Actavis Comments on Filing of DOJ Complaint - MarketWatch

13 November 2008, by

[edit] Lawbits - Legal Issues of Today » Blog Archive » Digitek Recall ...

12 November 2008, by LRanft The Digitek recall has been ignited because the manufacturer mistakenly produced tablets that were double in strength and has resulted in serious injury or death for many to date. Digitek is also known as Digoxin, Cardoxin, Lanoxicaps, ...

[edit] Digitek Inadvertently Caused Broken Ribs - Lawyers and Settlements

11 November 2008, by

[edit] Digitek’s Potentially Fatal Mistake Affects Many - St. Louis Post-Dispatch

7 November 2008, by

[edit] Digitek Lawyers Appointed to Leadership Roles in Federal MDL - AboutLawsuits.com

6 November 2008, by

[edit] "Didn't Realize the Danger of Digitek until it Happened to Me" - Lawyers and Settlements

4 November 2008, by

[edit] Hissey Kientz, LLP Announces the Launch of Digitek Recall Help Web Site

4 November 2008, by The law firm of Hissey Kientz, LLP has announced the launch of its new website, Digitek Recall Help (http://www.digitekrecallhelp.com). Digitek is a form of the heart medication digoxin, which is used to treat patients with an irregular heartbeat or congestive heart failure. ...

[edit] Digitek: Five Days Too Late - Lawyers and Settlements

29 October 2008, by

[edit] Congress Requests Information from FDA about Digitek Recall ...

10 October 2008, by admin The U.S. House Committee on Energy and Commerce has requested information from the FDA about a May 2008 Digitek recall issued by Actavis Totowa, as well as other regulatory issues involving the same generic drug maker in recent years. ...

[edit] Drug Injury Watch: Congress Will Investigate Digitek Recall And ...

9 October 2008, by Tom Lamb After Earlier Class 1 Recall Of Digitek, All Acvtavis Drugs Manufactured At Its Little Falls, NJ Plant Were Recalled In August 2008 (Posted by Tom Lamb at DrugInjuryWatch.com) On October 8, 2008 Representatives John D. Dingell (D-MI), ...

[edit] Digitek Recall: Generic drug maker reaps benefits of Digitek ...

5 October 2008, by Emily Marsh Many previous Digitek consumers have steered away from Digitek after the recall. However, as Digitek has lost consumers, Lannett Company has only reaped the.

[edit] Digitek Recall: MDL consolidates Digitek recall cases | Beasley Allen

28 September 2008, by Emily Marsh According to Huntington News, the United States Judicial Panel on Multidistrict Litigation (MDL) has ordered that all federal lawsuits about the double.

[edit] Digitek Recall Help Launched

24 September 2008, by Stem client Hissey Kientz LLP has launched a new website, Digitek Recall Help, that tracks the latest information regarding the recall of the heart medication Digitek, generically known as Digoxin. The site documents the related side effects, toxicity problems, lawsuits, and the latest news. It will function as an ongoing information gateway, updated regularly by the firm's Digitek practice group.

[edit] VLLB Linkblog: Digitek Recall Help Launched

23 September 2008, by Steve Matthews Stem client Hissey Kientz LLP has launched a new website, Digitek Recall Help, that tracks the latest information regarding the recall of the heart medication Digitek, generically known as Digoxin. The site documents the related side ...

[edit] Connie Crosby Links: Digitek Recall - New Website

23 September 2008, by Connie Steve Matthews of Stem Legal has announced his client Hissey Kientz LLP has launched a new website, Digitek Recall Help, that tracks the latest information regarding the recall of the heart medication Digitek, generically known as ...

[edit] Heart Surgery Patient Warning!!

6 September 2008, by Heart Surgery Patient Warning!!

[edit] Digitek Digoxin Recall Lawyer - The Law Office of Capretz & Associates, Attorneys at law

28 August 2008, by yyeroc

[edit] Actavis looking for documentation specialist

18 August 2008, by Maybe this is why we had the Digitek recall: They were short staffed. Performs quality related investigations and provides detailed reports for management review. Assesses impact of failures on surrounding lots, conducts process analysis to determine cause for failure and provides permanent corrective actions. Evaluates process deviations, out of trend reports, out of tolerance impacts and customer complaints. Source: Little Falls, NJ 07424-Documentation Specialist Technorati

[edit] Hissey Kientz Concerned That Patients Have Not Been Provided With Crucial Information About Digitek Recall Despite the D...

17 August 2008, by (PR News Releases News and Information) The law firm of Hissey Kientz LLP is concerned over recent reports that many heart patients may not have been fully informed by the drugs manufacturer about problems with the heart drug Digitek Drugmaker Actavis Totowa issued a nationwide recall ...

[edit] Hissey Kientz Concerned That Patients Have Not Been Provided With Crucial Information About Digitek Recall Despite the D...

16 August 2008, by Hissey Kientz, LLP is concerned that despite a recent recall notice for the heart drug Digitek, the drug’s manufacturer has failed to provide any additional information on how long the heart medication was being improperly manufactured. According to a press release issued by the manufacturer, ...

[edit] Hissey Kientz Concerned That Patients Have Not Been Provided With Crucial Information About Digitek Recall Despite the ....

16 August 2008, by Hissey Kientz, LLP is concerned that despite a recent recall notice for the heart drug Digitek, the drug’s manufacturer has failed to provide any additional information on how long the heart medication was being improperly manufactured. According to a press release issued by the manufacturer, ...

[edit] Actavis Totowa Finally Does The Right Thing

5 August 2008, by With such potentially dangerous drugs being produced, one would think the 2006 FDA report stating that 'Prompt action to correct all of the deficiencies' must be taken, and that 'Failure to promptly correct these deviations may result in regulatory action without further notice' would have yielded these results within a time frame much shorter than two full years. Instead, it took a second FDA inspection earlier this year and hundreds of potential lawsuits, for these products to finally be recal

[edit] Actavis Totowa Recalls all Drug Products from Little Falls Plant

4 August 2008, by Actavis Totowa Announces Voluntary Recall at the Retail Level of All Drug Products Manufactured at its Little Falls, New Jersey Facility FOR IMMEDIATE RELEASE — Morristown, NJ, August 1, 2008 — Actavis Totowa LLC, a generic drug manufacturer, is announcing a voluntary recall, to the retail level, of all drug products manufactured at its Little Falls, New Jersey facility. This is a precautionary, voluntary action by Actavis following an inspection conducted by the Food and Drug Administration

[edit] Denver Digitek Death Lawsuit Filed by Digitek Lawyers Klein | Frank, P.C

4 August 2008, by Digitek Death Lawsuit - Actavis Totowa Accused of Producing Dangerously Defective Digitek Heart Pills in Lawsuit Filed by Klein | Frank, P.C.   Denver, Colorado, August 1, 2008.  A lawsuit filed in United States District Court in Denver, Colorado on August 1, 2008 charges pharmaceutical company Actavis Totowa LLC with manufacturing and distributing defective Digitek heart drug pills that contained dangerously excessive doses of the drug’s active ingredient, digoxin, causing life-threatening

[edit] Digitek Dangers

1 August 2008, by Digitek Dangers By Janice Johnson On April 25, 2008 Digitek (digoxin), a medication used to treat congestive heart failure, abnormal heart rhythms, and other conditions, was recalled due to the possibility that tablets were doubled in thickness and could contain twice the approved level of the active ingredient. The existence of double-strength pills pose a risk of digitalis toxicity, which can result in nausea, vomiting, low blood pressure, cardiac instability, bradycardia and even death.

[edit] Digitek Digoxin Lawyers, Litigation and Frequent Questions

9 July 2008, by The manufacturer, Actavis Totowa, LLC has issued a press statement that responds, in part to frequently asked questions about the Digitek recall and the specific Digitek tablets that are at issue. Check your prescription for digoxin tablets manufactured by Actavis. The defective digoxin or Digitek products were distributed by: Mylan Pharmaceuticals, Inc. under the “Bertek” label UDL Laboratories, Inc. under the “UDL” label. OUr recommendation is that you or your representative visit your pha

[edit] US Drug Watchdog Expands Its National Investigation Into The Drug Called Digitek And Would Like To Talk To Possible Vict...

1 July 2008, by (Healthcare News and Information) Americas Watchdogs US Drug Watchdog has just expanded its national investigation into the drug called Digitek According to the Food Drug Administration FDA the Digitek defect could expose users to twice the amount of active ingredient which could cause ...

[edit] US Drug Watchdog Expands Its National Investigation Into The Drug Called Digitek, And Would Like To Talk To Possible Vic...

30 June 2008, by Americas Watchdog's US Drug Watchdog has expanded its national investigation of the drug called Diditek. In April 2008, Actavis Towtowa recalled all lots of Bertek and UDL Laboratories Digitek (digoxin tablets, USP, all strengths) for oral use, due to a manufacturing defect. Since that time ...

[edit] US Drug Watchdog Launches a National Investigation Into and Wants to Hear From Consumers About the Drug Called Digitek

25 June 2008, by (Hospitals News and Information) Americas Watchdogs US Drug Watchdog has just launched a national investigation into the drug called Digitek The Food Drug Administration FDA said The Digitek defect could expose users to twice the amount of active ingredient which could cause serious ...

[edit] LegalView Announced its Newest Information Portal with Details of the Digitek Digoxin Heart Tablet Recall

21 June 2008, by LegalView informed readers of its newest information portal detailing the U.S. Food and Drug Administration (FDA) ordered recall of the Digitek-brand digoxin heart tablets. The tablets had been recently discovered to have been manufactured containing twice the amount of active ingredient ...

[edit] Digitek's Double Dose Debacle

23 May 2008, by janevm Frank Grady suffers from atrial fibulation—a heart disorder that affects millions of people. Treatment usually comprises medication to slow a rapid heart rate. In Grady's case, he was given Digitek (digoxin), a drug so toxic that it can kill you if you

[edit] LegalView Reports of Woman Allegedly Fired For Expressing Concerns with AsbestosTainted Flooring At Her Workplace

23 May 2008, by (Cancer News and Information) LegalView the most comprehensive resource for everything legal on the Web recently offered readers updated mesothelioma information httpmesotheliomalegalviewcomblog through its mesothelioma blog The story concerns a woman who was allegedly fired for expressing her concerns ...

[edit] Generic heart drug Digitek recalled by Icelandic maker

19 May 2008, by By Catherine Larkin/Bloomberg News Actavis Group has recalled all lots of the generic heart drug Digitek because they may contain twice as much medicine as they should. “Several reports of illnesses and injuries have been received” in connection with the tablets, distributed by Mylan Laboratories Inc. under its Bertek and UDL brands, according to a notice posted Monday on the Food and Drug Administration’s Web site. Actavis has received 11 reports of side effects in about a year, though some

[edit] Digitek® (digoxin tablets, USP), manufactured by Actavis Totowa, has been linked to serious risk of Digitalis toxicity in those patients suffering from renal failure.

14 May 2008, by lacithomas ... used to treat heart failure as well as abnormal heart rhythms. Actavis has issued a Class I recall on the Digitek tablets because there is a possibility that tablets with twice the appropriate thickness might have...

[edit] Urgent Drug Recall on heart medication

12 May 2008, by Both humans and pets who are on this drug are being urged to contact your physician or veterinarian. This is listed on the US Drug Recall website so don’t tarry, WOOF! PERMISSION TO CROSS POST If you have or know of a dog or human family member currently on the heart med Digoxin there is [...]

[edit] Digitek Recall

9 May 2008, by Digitek Recall May 9, 2008 The FDA announced a recall for a brand of digoxin called Digitek. Digoxin is a heart medication and Digitek is often used by some pharmacy as the “generic” brand. The issue seems to be a dosing irregularity or inaccuracy. This can result in a person getting too much of the medication digoxin and possibly result in heart arrthymias. Therefore for those of you taking digoxin, you should check your prescription to see if your pills are covered under the recall. Most ph

[edit] Bad Medicine

8 May 2008, by   Good News/Bad News. If you are now currently taking the medicine Digitek then you have a very serious problem.  It appears that Digitek is bad news, at least right now it is, if you are taking it, you could be receiving a “DOUBLE DOSE” which is not going to be a fun ride.  A freind of mine in Denver, who is not a big fan of doctors and the medical profession in general. Will always comment to me when she hears about them screwing up with “that is why the call it PRACTICING MEDICINE the

[edit] Practicing Medicine

8 May 2008, by   Good News/Bad News. If you are now currently taking the medicine Digitek then you have a very serious problem.  It appears that Digitek is bad news, at least right now it is, if you are taking it, you could be receiving a “DOUBLE DOSE” which is not going to be a fun ride.  A freind of mine in Denver, who is not a big fan of doctors and the medical profession in general. Will always comment to me when she hears about them screwing up with “that is why the call it PRACTICING MEDICINE the

[edit] Urgent Digitek Recall

7 May 2008, by Urgent Digitek Recall WARNING: THIS DRUG (Digitek) MAY KILL YOU!!! I just learned today that a Class #1 recall has been issued on my Digitek heart medication! (Class I Recalls by the US Food and Drug Administration (FDA) are the most severe type of FDA recall. In a Class-I recall there is a potential for serious injury or death!!!). Do you know how I found out? I got a bill from my mail order pharmacy with my Digitek order marked CANCELED. Before I could place a call to find out why, I actua

[edit] Urgent Digitek Recall

6 May 2008, by WARNING: THIS DRUG (Digitek) MAY KILL YOU!!! I just learned today that a Class #1 recall has been issued on my Digitek heart medication! (Class I Recalls by the US Food and Drug Administration (FDA) are the most severe type of FDA recall. In a Class-I recall there is a potential for serious injury or death!!!). Do you know how I found out? I got a bill from my mail order pharmacy with my Digitek order marked CANCELED. Before I could place a call to find out why, I actually received an order

[edit] Drug Injury Watch: Extent Of Digitek Recall Remains A Mystery Ten ...

6 May 2008, by Tom Lamb Heart Medication Sold By Mylan Was Made In Actavis Plant That Received FDA Letter About Manufacturing Problems Over A Year Ago (Posted by Tom Lamb at DrugInjuryWatch.com) News about the April 2008 Digitek recall came first in the form ...

[edit] Urgent Digitek Digoxin Recall

6 May 2008, by FYI Urgent Digitek Digoxin Recall April 28, 2008 A class I recall is being issued on all Digitek (digoxin) tablets, which may contain twice the approved level of digoxin.The existence of double-strength pills pose a risk of digitalis toxicity, which can result in nausea, vomiting, low blood pressure, cardiac instability, bradycardia and even death. http://www.usrecallnews.com/2008/04/urgent-digitek-digoxin-recall.html Urgent News some Pharmacies are not sharing with the consumer, yet..

[edit] Digitek Recall by FDA

5 May 2008, by Several Brands of Heart Medication Recalled Heart problems and heart failure are two of the leading causes of death in the United States every year. As a result, pharmaceutical companies everywhere are placing a high priority on the research and development of medications that will provide relief and the ability to manage these conditions for [...]

[edit] Digitek Recall by FDA

5 May 2008, by Digitek Recall by FDA May 5th, 2008 Several Brands of Heart Medication Recalled Heart problems and heart failure are two of the leading causes of death in the United States every year. As a result, pharmaceutical companies everywhere are placing a high priority on the research and development of medications that will provide relief and the ability to manage these conditions for […] No Comments

[edit] Digitek Recall by FDA

5 May 2008, by Several Brands of Heart Medication Recalled Heart problems and heart failure are two of the leading causes of death in the United States every year. As a result, pharmaceutical companies everywhere are placing a high priority on the research and development of medications that will provide relief and the ability to manage these conditions for [...]