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Recall Lawsuit

Liquid Tylenol Recall

McNeil Consumer Healthcare has issued a voluntary recall of some its Children and Infant Liquid Tylenol Products that were manufactured between April of 2008 and June of 2008.

The Tylenol recall is a result of an inactive ingredient not meeting quality standards. The company pulled the product as a precautionary measure.

Children’s Tylenol, with the active ingredient is acetaminophen, has also faced an over-dose problem in regards to some of its Children’s and Infants Melt aways and Soft Chews. The design of the Melt away and Soft Chew packages include some blister voids that contain one tablet while some others contain two per void. Concern has been raised that the labeling on the carton and the back of the cavities that contain two tablets may lead the consumer to believe that two tablets provide a total of only 80mg when two-tablets are really a total of 160mg which, when consumed by a child, can lead to over-dosing. Although this problem is of much concern it is not the reason for the recent recall nor are the Melt aways or Soft Chew a part of this particular recall.

The following Children’s and Infant Tylenol products and lot numbers have been recalled:

  • Children's Tylenol Plus Cold MS Suspension 4 oz. Grape
    • SBM041, SBM067, SCM037, SDM027, SEM109
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Adderall Lawsuit

Adderall Side Effects Attorney


              Adderall is a drug used for the treatment of Attention Deficit

Hyperactivity Disorder, also known as ADHA. The drug is also indicated for

the treatment of Narcolepsy. Adderall is used as an fundamental part of a

complete treatment program, that may also include psychological, educational,

and social measures, for patients with ADHD. The drug treatment is not to be

used for all children with ADHD, for the syndrome may be secondary to primary

psychiatric disorders, including psychosis, and Adderall stimulants are not

intended for use in these patients.

              Attention Deficit Hyperactivity Disorder (ADHD; DSM-IV ®)

implies that hyperactive-impulsive or inattentive symptoms that caused

impairment are present and were present before the child was 7 years old. The

child’s symptoms have to cause clinically considerable impairment, for

example when functioning in academic, social, or occupational setting.

Symptoms must be present in two or more setting, such as

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Zicam Recall Lawsuit


              Earlier this summer the FDA stated that it had received 130 reports of anosmia, or loss of sense of smell, in users of three Zicam nasal cold remedies and warned consumers not to the products. The FDA alert lead to the recall of two of the products, Zicam Cold Remedy Swabs and Zicam Remedy Nasal Gel, by the makers of the product named Matrixx.

Matrixx had already withdrawn the third product named by the FDA, Zicam Cold Remedy Swabs for Kids. After the FDA issued the recall they learned of 800 more reports of Zicam problems that they were never notified of and they then issued a warning letter to Matrixx for withholding the information.  The warning letter also stated that the product could not be marketed without agency approval and that the nasal remedies did not include proper warnings about the risk of anosmia.

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Apotex Drug Recall

              Certain Lots of the Apotex drug’s, Apo-Amilzide, Apo-Meloxicam, and Apo-Ranitidine, have been recalled.

              Apo-Amilzide 5-50 mg is used to treat symptoms of osteoarthritis and rheumatoid arthritis in adults. Apo-Meloxicam 7.5 mg is used for patients with liver cirrhosis for maintenance therapy. Apo-Ranitidine 75 mg and 150 mg are used to help avoid problems associated with excess acid in the stomach. The recall affects on selected lots of these drugs.

The Three Products are on the Canadian market. Health Canada is conducting inspections in Toronto of Apotex manufacturing facilities. Health Canada is now also continuing with their inspections in Ontario Apotex facilities to determine whether manufacturing standards are being followed and to see if any other products are affected.

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