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SafetyAlerts
April 11, 2002

Horizon Laboratories Acti-Gest and Super Enzyme Recall Update

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
a) Acti-Gest Tablets, 150 mg/tab. Recall # F-345-2;
b) Super Enzyme Capsules, 50 mg/cap. Recall #F-346-2;
c) Super Enzyme Tablets, 50 mg/tab. Recall # F-347-2.

CODE
a) Lot 0101288;
b) Lot 0101284;
c) Lot 0101216.

RECALLING FIRM/MANUFACTURER
Horizon Laboratories, Inc., Chatsworth, CA, by letter on May 14, 2001.
Firm initiated recall is complete.

REASON
Contaminated with Salmonella spp.

VOLUME OF PRODUCT IN COMMERCE
Firm distributed all products manufactured.

DISTRIBUTION
CA
.

 
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?

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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.