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SafetyAlerts
August 23, 2001

Dynabac Tablets Recalled

Indianapolis, IN (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Eli Lilly and Company is recalling Dynabac tablets because of a related substance test failure at stability (12 Month).

This is the first public notice of this Class III recall issued by the FDA.

RECALL NUMBER, PRODUCT AND CODE:
D-268-1, (Rx) Dynabac tablets, delayed release (Dirithromycin) 250 mg, 10 and 60 count, eight various lots

MANUFACTURER/RECALLING FIRM:
Eli Lilly and Company, Indianapolis, IN

RECALLED BY:
By letter on May 15, 2001

FIRM INITIATED RECALL:
Ongoing

DISTRIBUTION:
Nationwide

QUANTITY:
52,060 -60 count
137,832 -10 count

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

 
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.