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

SafetyAlerts
August 8, 2002

Berlex Laboratories Has Recalled Quinaglute Dura-Tabs

(SafetyAlerts) - The FDA has released the following information.

PRODUCT
Quinaglute Dura-Tabs, Extended Release Tablets (quinidine gluconate, USP) 324 mg, 100, 250, and 500 count bottles, Rx. Recall # D-370-2.

CODE
Lot Numbers:
W00238 Exp. 11/2004
W00239 Exp. 12/2004
W00240 Exp. 1/2005
W10001 Exp. 3/2005
W10028 Exp. 4/2005
W10029 Exp. 5/2005
W10111 Exp. 7/2005.

RECALLING FIRM/MANUFACTURER
Berlex Laboratories, Inc., Wayne, NJ, by letters on July 23, 2002.
Firm initiated recall is ongoing.

REASON
Metal particles in tablets.

VOLUME OF PRODUCT IN COMMERCE
2,603 bottles of 100's; 3,358 bottles of 250's; 15,286 bottles of 500's.

DISTRIBUTION
Nationwide
.

 
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.

 

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.