Safety Alerts Saves Lives
Safety Alerts  
 
Home Privacy About Us Contact Us Change Preferences

SafetyAlerts
December 28, 1999

Purdue Frederick Co. Recalls Trilisate Tablets

Norwalk, CT (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that The Purdue Frederick Co. is recalling Trilisate Tablets, made by P.F. Laboratories because the product was found to be subpotent (choline content).

This Class III recall was initiated by the company by telephone between April 30, 1999, and May 7, 1999, and by letter during the week of May 3, 1999.  This is the first public notice issued by the FDA.  The FDA considers this recall to be complete.

The Trilisate Tablets (Choline Magnesium Trisalicylate), 750 mg, 500 count bottles, is a prescription non-sterodial anti-inflammatory, analgesic and anti-pyretic preparation. (NDC #0034-0505-50).  The recalled product bears LOT # 71G1 EXP 3/01.  Over 790 bottles were distributed nationwide.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

Sign-up for SafetyAlerts by Email -
The free internet newsletter that could
some day literally save your life - or
the life of someone you know.

Safety Alerts compiles comprehensive safety recall information for the United States. SafeMail is a free email service to warn consumers of faulty products and contaminated foods. For complete information regarding current recalls, past recalls and timely product warning notification visit: www.safetyalerts.com.

###

 

The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.