Safety Alerts Saves Lives
Safety Alerts  
Home Privacy About Us Contact Us Change Preferences
" "
Safety Alerts
August 4, 1999

UDL Laboratories, Inc. Recalls Atenolol Tablets and Robot Ready Cards

Rockford, IL (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that UDL Laboratories, Inc. is recalling Atenolol Tablets and Robot Ready Cards (Aminocaproic Acid) because of content uniformity failure.

Atenolol Tablets, USP, 25 mg, in unit dose packages of 100 (10 strips/10 tablets) and Robot Ready Cards (25 cards of 1 tablet), Rx oral beta-selective beta-adrenergic receptor blocking used in the management of hypertension and angina pectoris. NDC #51079-759-20 and NDC #517079-759-19.

Recall #D-290-9.

Lot Numbers: 9B254, 9A124, 8M577, 8P694.

Lederle Pharmaceutical, Division of American Cyanamid,Pearl River, New York.

UDL Laboratories, Inc., Rockford, Illinois, by letter dated June 25, 1999. Firm-initiated recall ongoing.


27,394 unit cartons of 100 tablets and 1,582 unit cartons of 25 tablets were distributed; firm estimated that 20 percent of the products remained on market at time of recall initiation.


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.