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AddThis Social Bookmark Button Actavis Totowa Generic Drug Recall Lawyers ------------------------------------------
Keywords: Actavis Drug Recall Lawyer Lawsuit The lawyers and attorneys at our firm are currently offering free case evaluations to individuals injured by defective generic drugs manufactured by Actavis Totowa LLC at its Falls River, New Jersey facility. On August 1, 2008, Actavis Totowa recalled all generic drugs made at that facility because of manufacturing issues. If you believe you suffered an adverse reaction from one of these recalled medications, we urge you to contact one of our Actavis Totowa generic drug recall lawyers as soon as possible to protect your rights.
The Actavis Totowa generic drug recall lawyers at our firm have learned that the company's Falls River, New Jersey manufacturing plant has been the subject of numerous safety issues in the past. This includes one other drug recall, as well as a warning letter issued by the Food & Drug Administration (FDA) in 2007 regarding inadequate conditions at the plant. Clearly, the fact that Actavis Totowa has found it necessary to recall every medication made at Falls River indicates that previous safety problems were not adequately addressed. Our Actavis Totowa generic drug recall lawyers intend to hold this company responsible for this failure. Actavis Totowa Generic Drug Recall
The Actavis Totowa generic drug recall was initiated after an inspection of the facility revealed that operations did not meet the FDA’s standards for good manufacturing practices. Actavis Totowa asked pharmacies, hospitals and retailers to return the affected prescription medications. The Actavis Totowa generic drug recall was initiated at the retail level only, and patients were not told to discard of their potentially defective medications. Both the company and the FDA have maintained that the recall is precautionary, and that no injuries have been reported as a result of the defective generic drugs. However, the vast majority of adverse drug reactions are never reported, and our Actavis Totowa generic drug recall lawyers believe that it is entirely possible that these shoddy medications have already injured many people.
The Actavis Totowa generic drug recall involved dozens of medications. The drugs recalled were: Amantadine 100mg capsules
Amibid DM ER tablets Amibid DM tablets
Amidrine capsules Amigesic 500 mg caplets and 750 mg caplets
Amitex PSE tablets Bellamine S tablets
Betaxolol 10 mg and 20 mg tablets USP Buspirone HCL 5 mg, 10 mg, 15 mg and 30mg tablets
Carisoprodol & Aspirin tablets Carisoprodol, Aspirin & Codeine tablets
Carisoprodol 350mg tablets Chlordiazepoxide w/ Clidinium Bromide capsules
Chlorzoxazone 250mg Cilostazol tablets 100mg
Choline Magnesium Trisalicylate 500 mg, 750 mg and 1000 mg tablets Cyclobenzaprine HCL 5 mg and 10 mg
Dexchlorpheniramine Maleate 4 mg and 6 mg tablets Dipyridamole 25 mg, 50mg, and 75 mg tablets
Glyburide 1.5 mg, 3.0 mg and 6.0 mg tablets Guaifenesin & Codeine Phosphate tablets
Guaifenesin & Phenylephrine tablets Guanfacine 1.0 mg and 2.0 mg HCl tablets
Hydrocodone & Homatropine tablets Hydromorphone HCl tablets
Hydroxyzine 10 mg, 25 mg and 50 mg tablets Hyoscyamine Sulfate 0.125 mg SL
Hyoscyamine Sulfate 0.375mg SR tablets Hyoscyamine Sulfate 0.125 mg (oral) tablets
Isradipine 2.5 mg and 5 mg capsules Loxapine 5 mg, 10 mg, 25 mg, and 50 mg capsules
Meclizine Chewable 25 mg tablets Meloxicam 7.5 mg and 15 mg tablets
Meperidine & Promethazine capsules Meperidine HCl 100 mg and 50 mg tablets
Methenamine Mandelate 0.5 g and 1.0 g tablets Mirtazapine 15 mg, 30 mg, and 45 mg tablets
Mirtazapine OD tablets, 15 mg, 30 mg and 45 mg Multi-ret Folic 500 mg tablets
Multi-vita-bets 0.5 mg and 1.0 mg FL & FE tablets Multi-vita-bets 0.25 mg, 0.5 mg and 1 mg FL tablets
Naltrexone 50mg tablets Oxycodone & Acetaminophen 5/500mg capsules
Oxycodone HCl 5 mg, 15 mg and 30 mg tablets Oxycodone HCl 5 mg capsules
Pentazocine & Acetaminophen tablets Pentazocine & Naloxone tablets
Phenazopyridine HCl 100 mg and 200 mg tablets Phendimetrazine Tartrate 35mg tablets
Phentermine HCl 37.5 mg tablets Phentermine HCl 15 mg, 30 mg and 37.5 mg capsules
Prenatal Formula 3 tablets Prenatal Plus 27 mg FE tablets
Prenatal Rx tablets Quinaretic 10mg/12.5mg, 20 mg/12.5 mg and 20 mg/25 mg tablets
Rifampin 300mg capsules Sodium FL 0.5 mg and 1.0 mg tablets
Tizanidine HCl 2 mg and 4 mg tablets Trimethobenzamide 300mg capsules
Trimipramine Maleate 25mg, 50mg, 100mg capsules Trivita 1 mg FL tablets
Ursodiol capsules, 300mg Vitacon Forte capsules
Vitaplex Plus tablets Vitaplex tablets (FC)
Yohimbine HCl 5.4 mg tablets If you or someone you know have taken any of these recalled medications and suffered a side effect or injury, we urge you to contact one of our Actavis Totowa generic drug recall lawyers right away.
Previous Actavis Totowa Safety Problems Actavis Totowa has had a history of safety problems. Months before its generic drug recall, in April 2008, Actavis recalled Digitek tablets because some of the medication contained twice the active ingredient normally found in Digitek. According to the FDA, the Digitek defect could cause serious and even fatal digitalis reactions in users. Some of the faulty Digitek tablets involved in this earlier recall were made at the New Jersey facility.
The FDA deemed the Digitek recall a Class I recall, meaning that the defective Digitek tablets could cause serious health problems or death. According to the agency, there have been several reports of illnesses and injuries in patient taking Digitek. Actavis said it had 11 such reports. But because not all adverse reactions are reported to the FDA or manufacturers, the true number could be much higher. In February 2007, the FDA issued a warning letter to Actavis Totowa following an inspection of the Little Falls facility completed in August 2006. The violations cited in that letter included: significant deficiencies in the company's quality control unit; laboratory notebooks that did not include all raw test data generated during testing; failure to check for accuracy the inputs to and outputs from the "Total Chrom Data Acquisition System," which was used to run the firm's HPLC instruments; quality control failed to recognize that some tablets that did not meet in-process specifications; lack of adequate procedures for conducting bulk product holding time studies; cleaning validation studies were found to be inadequate; master and batch production and control records were found to be deficient; and equipment used in the manufacture of Benztropine Mesylate tablets and other drug products was not adequately qualified.
In the warning letter, the FDA stated that it had reviewed the firm's corrective actions promised in a letter dated Aug. 29, 2006. The agency found that while corrections the firm promised in its correspondence appeared to adequately address many of the violations, the FDA reiterated its concern about the quality of drug products that were released from the facility under the serious lack of controls found during the inspection. Legal Help for Victims of Defective Actavis Totowa Generic Drugs
If you or a loved believe you were injured by a defective generic drug recently recalled by Actavis Totowa, you have valuable legal rights. Please fill out our online form or call 1-800-LAW-INFO (1-800-529-4636) to discuss your case with an experienced Actavis Totowa generic drug recall lawyer. Actavis RecallRSS Feed
Actavis Reopens Plant Closed After Digitek, Other Drug Recalls Apr 20, 2009 Parker Waichman Alonso LLP
Actavis Totowa has received approval from the Food & Drug Administration (FDA) to reintroduce Oxycodone tablets made at its Little Falls, NJ facility. The Little Falls plant was one of three closed last year following recalls of oversized Digitek (Digoxin) tablets and other defective generic drugs.Actavis agreed to temporarily close its Little Falls manufacturing facility, as well as another in Riverview and a packaging plant in Taft as part of a Consent Decree it reached with federal... Actavis Reopens Plant Closed After Digitek, Other Drug Recalls » Following Digitek, Other Drug Recalls, Feds Seek to Shutter Actavis Facilities
Nov 18, 2008 Parker Waichman Alonso LLP Actavis Totowa, LLC, the maker of defective Digitek tablets, now faces a lawsuit filed by the U.S. Justice Department that seeks to shut down substandard manufacturing plants in New Jersey. In April 2008, Actavis Totowa recalled Digitek tablets because some of the medication contained twice the active ingredient normally found in Digitek. According to the Food & Drug Administration (FDA), the Digitek defect could cause serious and even fatal reactions in users. The FDA... Following Digitek, Other Drug Recalls, Feds Seek to Shutter Actavis Facilities »
Digitek, Other Generic Drug Recalls Prompt Congressional Probe of Actavis Totowa Oct 10, 2008 Parker Waichman Alonso LLP
Actavis Totowa, the company that has recalled a variety of drugs this year, including Digitek tablets and fentanyl patches, has attracted the attention of lawmakers on the House Energy and Commerce Committee. Chairman John Dingell (D-Mich.) and Oversight and Investigations Subcommittee Chairman Bart Stupak (D-Mich.) have sent a letter to the Food & Drug Administration (FDA) seeking information about the Actavis recalls. In April 2008, Actavis Totowa recalled Digitek tablets because... Digitek, Other Generic Drug Recalls Prompt Congressional Probe of Actavis Totowa » Suit Over Phenytoin Names 10 Defendants in Womans Death
Aug 15, 2008 Parker Waichman Alonso LLP According to court papers, Agnes Davis was prescribed phenytoin and then suffered a severe adverse reaction- Stevens-Johnson Syndrome - that allegedly led to her death. Phenytoin is a generic version of Dilantin. The lawsuit, filed by Willie Davis Jr. and Alice Washington—Davis’s family members—on August. 8, 2008, names 10 companies that make, label, test, market, or distribute phenytoin. Among other issues, the defendents allege that the defendants misled... Suit Over Phenytoin Names 10 Defendants in Womans Death »
CEO Leaves Actavis Group Aug 6, 2008 Parker Waichman Alonso LLP
Just days after its U.S. division recalled all of its generic drugs, Icelandic drug maker Actavis Group announced that its CEO is stepping down. However, in announcing the departure of Róbert Wessman, the company made no mention of Actavis Totowa's recent safety problems, which also included an April recall of Digitek tablets.Instead, media reports say Wessman was stepping down to focus on his investment company Salt Investment, but will continue to have a seat on the board... CEO Leaves Actavis Group » More Actavis Recall News
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