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Safety Alerts
August 4, 1999

Glenwood, LLC Recalls Yodoxin 650 mg Tablets

Piscataway, NJ (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Glenwood, LLC is recalling Yodoxin 650 mg Tablets because of subpotency (6 month stability).

PRODUCT
Yodoxin 650 mg Tablets (lodoquinol USP), in 100 tablet bottles, Rx anti-amebic. NDC #0516-0093-01.

Recall #D-297-9.

CODE
Lot #49835 EXP 9/2001.

MANUFACTURER
Glenwood, LLC, Piscataway, New Jersey.

RECALLED BY
Manufacturer, by letter on February 22, 1999. Firm-initiated recall ongoing.

DISTRIBUTION
Nationwide.

QUANTITY
976 bottles were distributed.

 

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.