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

SafetyAlerts
July 24, 2002

Mikart Has Recalled Esgic-Plus Capsules

Atlanta, GA (SafetyAlerts) - The Food and Drug Administration (FDA) said that Mikart has recalled Esgic-Plus Capsules (Butalbital, Acetaminophen and Caffeine
Capsules, USP).

PRODUCT
Esgic-Plus Capsules (Butalbital, Acetaminophen and Caffeine Capsules, USP) 50 mg/500 mg/40 mg, 100 and 500 count bottles, Rx only, NDC# 0456-0679-01 and 0456-0679-02. Recall # D-352-2.

CODE
Lots D010201A, D010202A, D010203B, J010602A, J010603B and L010742A

RECALLING FIRM/MANUFACTURER
Mikart, Inc. Atlanta, GA, by phone and fax on April 30, 2002. Firm
Initiated recall ongoing.

REASON
Low weight dosage units.

VOLUME OF PRODUCT IN COMMERCE
23,081/100 ct. bottles;
966/500 ct. bottles.

DISTRIBUTION
MO
.

 
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.