ADVERTISEMENT



Google       

Home -> Law Blog Directory -> Legal News Blogs -> FindLaw's Common Law

OR PHONE (866) 635-1838 for Bankruptcy Help, (866) 635-6190 for Divorce,
(866) 635-2689 for Personal Injury or (866) 635-9402 for Criminal Defense

Find a Local Lawyer

Bankruptcy (866) 635-1838
Divorce (866) 635-6190
Personal Injury (866) 635-2689
Criminal Defense (866) 635-9402

Bookmark

Legal News

: FindLaw's Common Law

Johnson and Johnson, FDA Recall Some Children's Pain and Allergy Meds

ADVERTISEMENTS

Late on Friday, April 29, Johnson & Johnson and McNeil Consumer Healthcare announced a recall of several of their products, including liquid infant's and children's Tylenol, Motrin, Zyrtec, and Benadryl. A statement from FDA Commissioner Dr. Margaret Hamburg urged consumers to discontinue using the recalled products.

According to a report by Reuters, Hamburg's statement also said the potential for health problems to be caused by the recalled drugs is remote, however, "Americans deserve medications that are safe, effective and of the highest quality. We are investigating the products and facilities associated with this recall and will provide updates as we learn more," she said.

The recalled products were manufactured by McNeil Consumer Healthcare. The company has posted a full list of the affected products on its website which you can visit by clicking here.

According to the FDA press release, McNeil Consumer Health Care initiated the recall because some of the products may not meet required quality standards. Some of the products included in the recall may contain a higher concentration of active ingredient than specified; others contain inactive ingredients that may not meet internal testing requirements and others may contain tiny particles. The FDA is asking parents and caregivers to discontinue using these products. The generic versions of the products are not affected by the recall and are safe to use.

If a child has any adverse affects after using any of the recalled products, parents and caregivers can report the problems to FDA's MedWatch Adverse Event Reporting program either online, by regular mail, or by fax. The FDA asks health care professionals and consumers to report any adverse reactions to the FDA?s MedWatch Program by fax at 1-800-FDA-0178; by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787; or on the MedWatch website at: http://www.fda.gov/Safety/MedWatch/ucm2005699.htm. 

Consumers with questions about the recall can contact the company at 1-800-222-6036 or visit the website at: http://www.mcneilproductrecall.com/.

Related Resources:


Full post as published by FindLaw's Common Law on May 04, 2010 (boomark / email).

Bloggers, promote your law blog by nominating your blog for inclusion in USLaw.com's Law Blog Directory and RSS Reader. Benefits described.
Related Law Articles

Lawsuits and Settlements

Related Searches

























































































































US Law
#1 Online Legal Resource













Your Blog Subscriptions
Subscribe to blogs

10,000+ Law Job Listings
Lawyer . Police . Paralegal . Etc
Earn a law-related degree
Are you the author of this blog? Adding USLaw.com to your Blogroll increases relevance. You qualify to display a USLaw Network badge.
Suggest changes to this blog's description or nominate another for inclusion. Register for updates.


Practice Area
Zip Code:

Contact a Lawyer Now!






0.0199 secs (new cache)