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.