• Home
• About New York Injury News
• New York Lawyer Panel
• New Jersey Injury Lawyers
• Long Island Personal Injury Lawyers
• Ask A Lawyer
• News Tags

• Construction Accidents
• Injury News
• Medical Malpractice
• Motor Vehicle Accidents
• Personal Injury Accidents
• Premises Liability
• Product Liability
• Work Related Fire Fighter Deaths
• Wrongful Death

UPDATE: Johnson & Johnson files Tylenol consumer complaints late

Legal news for New York product liability attorneys— McNeil Consumer Healthcare’s agency filed consumer complaints a year later.

New York, NY (NewYorkInjuryNews.com) –The U.S. Food and Drug Administration (FDA) www.fda.gov has announced that McNeil Consumer Healthcare’s Johnson & Johnson unit should have taken action to recall Tylenol and other over-the-counter products after filed complaints of a strange smell of the product, according to the Wall Street Journal.

The FDA’s office of compliance sent the company a letter informing them of the violation of agency reporting rules and manufacturing practice rules. Consumers had been complaining about a mildew, moldy smell coming from the products in September 2008, and the agency did not begin a full investigation into the problem or report the complaints to the FDA until September 2009.

Friday, January 15, 2009, McNeil Consumer Healthcare expanded the recall to more than just Tylenol, but also recalled several other products such as Benadryl, Motrin, St. Joseph’s Aspirin. There were also complaints of musty-smelling Rolaids. There were consumer reports of nausea and temporal stomach issues due to use of the medication.

Investigations revealed that the moldy smell was linked to traces of a chemical that is applied to wood pallets used to ship the products. The company first recalled the Tylenol products in November 2009, simultaneously; the FDA was inspecting one of the agency’s plant in Puerto Rico. The FDA reported that, with the expanded recall, there were 50 million bottles recalled. It was noted that in 2009, Tylenol made up about $1 million in sales across the country. A report released by company, which stated that it failed to test if the Tylenol was contaminated, even after numerous consumer complaints.

The FDA is currently investigating the matter to determine if other companies use wooden pallets that contain this chemical. “All drug manufacturers have a corporate responsibility to ensure their products are high quality, safe and effective,” reported an official.

Bridget Hom

www.NewYorkInjuryNews.com

Related posts

• FDA alerts healthcare workers-topical pain meds before mammograms (0)
• FDA requires black box warning-Reglan may cause permanent injury! (0)
• FDA recalls Brooklyn diet pill company’s harmful over the counter supplements (0)
• FDA orders Botox makers place boxed high injury warning label - New York product injury Alert! (0)
• New Jersey drunk driver victimizes 7 innocent bystanders (0)
• Major NY car wreck kills 3, injures 1 (0)
• New York taxi cab crashes into local festival injuring 13 pedestrians (0)
• Boston, Massachusetts Work-Related Firefighter Bulletin - alarm blaze at boathouse (0)
• Vermont SUV rollover notice - Toddler killed in SUV accident on expressway (0)
• New York Motor Vehicle Accident Causes Head Trauma! (0)