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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.

PRODUCT
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.

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

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

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

DISTRIBUTION
Nationwide.

QUANTITY
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.