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SafetyAlerts
July 26, 2001

Vintage Pharmaceuticals Inc. Recalls Oxycodone HCL/Acetaminophen

Charlotte, NC (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Vintage Pharmaceuticals, Inc. is recalling certain lot(s) of Oxycodone HCL/Acetaminophen because of dissolution failure (Acetaminophen)

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

PRODUCT:
Oxycodone HCL/Acetaminophen 5/500 mg Rx Capsules under the Vintage and Qualitest labels. The product is packaged in 100 capsule bottles.

Recall Number: D-250-1

Code: Lot 126060A and 126060B

MANUFACTURER/RECALLING FIRM:
Vintage Pharmaceuticals, Inc., Charlotte, NC

RECALLED BY:
Vintage by letter on 2/13/01

DISTRIBUTION:
Nationwide

FIRM INITIATED RECALL:
Ongoing

DISTRIBUTION:
Nationwide

QUANTITY:
9,425 bottles

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

Notice of this product warning was sent via email to SafetyAlerts subscribers July 26, 2001.  For more information regarding the SafetyAlerts free email alert service please click here.

 
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.