Search for: "Actavis Totowa, LLC"
Results 1 - 20 of 30
Sorted by Relevance | Sort by Date
14 Nov, 2008 3:23 pm
... S. Regulators to Shut Heart Drug Manufacturer", got our attention due to the fact that this drug company, Actavis Totowa
LLC, was responsible for the April 2008 Digitek recall as well as an August 2008 recall of all other generic drugs ... attack FDA; call for
Obama to 'clean house'", Representative Bart Stupak said the Complaint for an injunction stopping Actavis from manufacturing generic drugs at
its Little Falls, New Jersey facility is "posturing" by FDA political appointees who have initiated ...
5 Aug, 2008 12:12 am
... , improper manufacturing of drug products may have occurred for some time. In early 2007, the FDA sent Actavis a warning letter after its
inspection showed that drug products manufactured in the facility were adulterated. The FDA criticized this ... associated with the drug products manufactured at the New Jersey
facility, all of which are prescription medications. According to the Actavis Totowa LLC press
release posted by the FDA, the recall took place because of operations "which did not meet the ...
28 Jul, 2008 9:31 pm
... effects as a result of taking Digitek, a recently recalled pharmaceutical drug designed as a heart medicine manufactured by Actavis
Totowa LLC. The medicine also known as Digoxin, is distributed by Mylan Pharmaceuticals, according to this news report. Earlier this
year, Actavis Totowa LLC recalled all lots Digitek because the tablets contained twice the
approved level of the active ingredient. The lawsuit states that there have been at least 11 complaints ...
29 Dec, 2008 12:47 pm
... Integrity (the Center, for short). The most surprising part of that article, to me, was this contention by the drug company: Actavis
maintains that none of the improperly manufactured Digitek pills ever reached the public, telling the Center that ... Decree of Permanent Injunction with the Food and Drug
Administration (FDA) regarding the company's Actavis Totowa LLC subsidiary. This agreement, in
effect, settles the issues identified by the Department of Justice in its previously filed complaint ...
4 Aug, 2008 8:05 pm
... sky is falling for some generic drug companies. On August 1, 2008 Actavis Totowa LLC
announced a recall of all generic drugs manufactured at its Little Falls, New ... Products Manufactured at its Little Falls, New Jersey Facility [Press Release] At this time,
Actavis only wants pharmacies and hospitals to return the prescription generic drugs that were ... FDA Class 1 Digitek Recall, We Have Been
Told Little About Actavis Manufacturing Problem". More generally, in mid-July 2008 I posted an article, "FDA ...
23 Jun, 2008 11:55 am
... release from Actavis which first announced and explained the Digitek recall: Morristown, NJ, 25 April, 2008 - Actavis Totowa LLC, a United States manufacturing division of the international generic pharmaceutical
company Actavis Group, is initiating ... at a more serious issue, that of accountability and liability for those defective Digitek pills. Who
is the responsible party, Actavis or Mylan or both? According to a June 12, 2008 article, "Families Suing Mylan For Medication Mistake",
published ...
9 Oct, 2008 3:59 pm
... spring of 2008 as well as the August 1, 2008 recall of all generic drugs manufactured at the Actavis Totowa LLC at its plant in Little Falls, New Jersey (formerly operated by Amide Pharmaceuticals). From the October 8 ... for the spring 2008 Digitek recall, and go
on to explain the basis for this Congressional investigation of what the FDA knew about Actavis manufacturing problems and when the agency knew
it: That drug was recalled "due to the possibility that tablets with double the appropriate ...
14 Aug, 2008 2:32 am
Sixty-five different potentially dangerous generic drugs manufactured by Actavis Totowa, LLC,
one of the world's largest generic drug manufacturers, were recalled from market last ... ; Vitaplex tablets (FC); and Yohimbine HCl 5.4 mg tablets. Actavis Capsules : Amantadine 100mg capsules; Amidrine capsules; Amigesic 500 mg caplets and ... manufacturing and poison the patient taking the pill.) No
word yet if this new Actavis drug recall poses the same threat to patients taking these recalled generic pills ...
26 Sep, 2008 7:23 pm
... . As you may recall, in late April 2008 the FDA announced that Digitek (digoxin tablets) manufactured by Actavis Totowa
LLC at its Little Falls, New Jersey plant was the subject of a nationwide Class I recall because of the possibility that some ... were
manufactured such that they contained twice the approved level of active ingredient. Furthermore, on August 1, 2008 Actavis Totowa
LLC announced a recall of all generic drugs manufactured at its Little Falls plant, apparently due to a lack of good ...
28 Jul, 2008 10:36 am
... Pearson's report - it's copyrighted: Digitek is the trade name for digoxin tablets manufactured in the United States by Actavis
Totowa, LLC, the U.S. manufacturing division of international generic pharmaceutical company Actavis Group. The tablets are ... "[t]hese tablets may contain twice the approved level of active ingredient than is appropriate." Further, according to the
Actavis Press Release: The existence of double strength tablets poses a risk of digitalis toxicity in patients with renal ...
25 Jul, 2008 11:56 pm
... the #1 choice for treating congestive heart failure and abnormal heart rhythms in the United States. On April 25, 2008, Actavis
Totowa LLC, the U.S. manufacturing division of the generic pharmaceutical company Actavis
Group, voluntarily initiated a Class ... label and by UDL Laboratories, Inc. under a "UDL" label.The voluntary recall of the Digitek tablets manufactured at the New Jersey
Actavis facility occurred because tablets may have been commercially released in the U.S. market with double the ...
5 Aug, 2008 1:40 am
... -based discrimination case - The blogging constitutionalists at the American Constitution Society at their ACS Blog Update on pharmaceutical giant Actavis Totowa LLC - Bryan Lester at Heygood, Orr, Bartolomei, Reyes & Bartolomei at the firm's Angel
Reyes Blog Does the manager of an LLC have a fiduciary duty to the members of the LLC? - Greensboro
lawyer Mack Sperling of Brooks Pierce LLP in his blog, the North Carolina Business Litigation ...
30 Apr, 2008 2:18 pm
... MedWatch Safety Alert came several days after a press release about this Digitek manufacturing problem was issued by Actavis Totowa
LLC (formerly known as Amide Pharmaceutical Inc). Therein, the manufacturer said it is recalling all strengths of ... their doctor if they have
any concerns or questions. P.S. According to a brief newspaper article dated April 25, 2008, "Digitek heart drug recall": [Actavis
Totowa LLC spokesman] John LaRocca said 11 people have reported getting sick after taking the ...
12 May, 2008 8:59 am
... notice": Urgent: Drug Recall -- Digitek® (digoxin tablets, USP) Recall initiated by the manufacturer: Actavis Totowa LLC (formerly known as Amide Pharmaceuticals, Inc.) Product Distributed by: Mylan Pharmaceuticals, Inc. under a " ... announcements by Actavis and the FDA: Mylan Pharmaceuticals Inc. is continuing a voluntary recall of the Actavis Totowa recall
of Digitek® (digoxin tablets, USP). This product is being recalled due to the possibility that tablets with double the appropriate thickness ...
29 Oct 3:13 am
... Lone Pine order. See generally Lore v. Lone Pine, No. L-336006-85, 1986 WL 637507 (N.J. Super. Ct. Nov. 18, 1986). Dozens of product liability cases alleging that defendants
Actavis Totowa LLC, Actavis Inc. and Actavis Elizabeth LLC marketed Digitek tablets containing double the appropriate dosage were transferred to an MDL
assigned to Chief Judge Goodwin of the Southern District of West Virginia last summer. In Re: Digitek Products Liability Litigation, ...
20 Jun, 2008 6:13 pm
... taking cases for individuals who have suffered injuries due to Digitek, also known as Digoxin. Recently, a drug manufacturer, Actavis
Totowa LLC, a United States manufacturing division of the international generic pharmaceutical company Actavis Group, has initiated a ... by Mylan Pharmaceuticals Inc., under a "Bertek" label and by UDL Laboratories, Inc. under a "UDL" label. Actavis manufactures the products for Mylan and the products are distributed by Mylan and UDL under the Bertek and UDL labels. ...
16 Oct, 2008 7:17 pm
... 60 mg Morphine Sulfate Extended Release Tablets made during a two-year period, June 2006 To May 2008. As you may know already, in April 2008 Actavis Totowa LLC recalled all strengths of Digitek due to the possibility that tablets with double the
appropriate thickness may ... numerous personal injury and wrongful death Digitek lawsuits have been filed against Actavis. As I have asked
rhetorically in the recent past: Where is the FDA on taking steps to ascertain that Good Manufacturing Practices ...
4 Nov, 2008 6:18 am
... , 2008, in Charleston. Digitek, also known as digitalis or digoxin, is a prescription drug that was recalled from the market in April of 2008 by manufacturers Actavis Totowa, LLC; Actavis, Inc.; Actavis US; Mylan, Inc.; Mylan Pharmaceuticals, Inc.; Mylan Laboratories, Inc.; Mylan Bertek Pharmaceuticals; and UDL Laboratories, Inc. Currently, more than
50 lawsuits have been filed against these manufacturers alleging personal injuries ...
13 Sep, 2008 1:16 am
Actavis Totowas LLC., manufacturer of the recalled defective heart drug Digitek, has announced
a voluntary recall of all drug products manufactured in its Little Falls, NJ facility. According to an alert posted by the U.S. ... the conditions at the facility to be less than
satisfactory. Hundreds of heart patients around the country have filed complaints against Actavis alleging that its heart drug, Digitek, also
known as Digoxin, caused severe side effects because of its dangerous drug dosage. The ...
21 Apr 2:34 am
... even a year has passed since the massive recall of Digitek pills by Bertek/Mylan and Actavis, yet cardiac patients are facing yet another
scare. On March 31, 2009, Caraco Pharmaceutical Laboratories ... may contain an excessive dose of the active ingredient of the medication. A similar massive recall was announced by
Actavis Totowa LLC, Mylan Bertek and UDL on April 25, 2008, involving millions of pills that
were improperly manufactured at a facility in Little Falls, New Jersey, which has been the ...
Search on: Blawgs.FM | BlawgSearch Google Co-op | Blawg.com | Bloglines | Feedster | Google Blog Search | Technorati | Google | MSN | Yahoo!