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SafetyAlerts
March 29, 2002

Aloe Flex Enterprises Weider's Eyedrops Recall Update

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

PRODUCT
Weider's Eyedrops (Aloeflex) NET WT. 1 fl. oz. (Aloe Vera juice). Recall # D-205-2.

CODE
Product is not coded, or if coded, coding is unknown. All codes were recalled.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Aloe Flex Enterprises, Dickinson, TX, by letter dated December 11. 2001;
Manufacturer: Tennis Elbow Corporation, Dickinson, TX.
FDA initiated recall is complete.

REASON
Microbial contamination (Acinetobacter calcoaceticus-baumannii).

VOLUME OF PRODUCT IN COMMERCE
28.

DISTRIBUTION
TX
.

 
Selected Recent Recalls


Health Professional:

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

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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.