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FOOD AND DRUG ADMINISTRATION
FOR IMMEDIATE RELEASE

Consumer Media: 888-Info-FDA
April 14, 1999

Mikart Inc. Recalls Bidex Tablets

PRODUCT
Bidex Tablets (Guaifenesin 800 mg) in 100 tablet bottles, Rx indicated for the temporary relief of coughs associated with respiratory tract infections, and related conditions such as pharyngitis, bronchitis, and asthma. NDC #45985-637-01. Recall #D-165-9.

CODE
Lot #J980755A.

MANUFACTURER
Mikart Inc., Atlanta, Georgia.

RECALLED BY
Manufacturer, by letters on March 10 and 24, 1999. Firm-initiated recall ongoing.

DISTRIBUTION
Alabama, Florida, Georgia, Illinois, Kentucky, Louisiana, Mississippi, Missouri, Nevada, North Carolina, Pennsylvania, Tennessee, Texas, Virginia.

QUANTITY
2,910 bottles were distributed.

REASON
Foreign particles - Carbon from raw material filtering.

 

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.