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

SafetyAlerts
July 24, 2002

Bristol-Myers Squib Has Recalled Desyrel Tablets

Evansville, IN (SafetyAlerts) - The Food and Drug Administration (FDA) said that Bristol-Myers Squibb Co. has recalled Desyrel Tablets (trazodone HCL tablets, USP).

PRODUCT
Desyrel Tablets (trazodone HCL tablets, USP), 100 mg, Rx only, packaged in bottles of 100 tablets(NDC 0087-0776-41) and 1,000 tablets (NDC 0087-0776-43). Recall # D-343-2.

CODE
2 Lots MLS08 and MKC09.

RECALLING FIRM/MANUFACTURER
Bristol-Myers Squibb Co., Evansville, IN, by letters on June 11, 2002.
Firm Initiated recall ongoing.

REASON
Lack of content uniformity-subpotent at 18 month stability.

VOLUME OF PRODUCT IN COMMERCE
2 Lots MLS08 and MKC09.

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.