July 26, 2001Vintage Pharmaceuticals Inc.
Recalls Q Tuss Tablets
NC (SafetyAlerts) - The Food and
Drug Administration (FDA) said today that Vintage Pharmaceuticals, Inc. is recalling
certain lot(s) of Q Tuss Tablets because of super-Potency (Scopolamine).
This is the first public notice of
this Class II
recall issued by FDA.
Q Tuss Tablets in bottles of 100's and 500's. The product is under the Zenith Goldline,
URL, QT, VPI and URL label.
Lots - 010079A, 010079B, 010079C,
097089A, 098089A, 098089B, 098089C, 098089D, 098089E, 098089F, 099089A, 099089B, 136039A,
136039B, 136039C, 136039D, 008119A, 010119A, 011119A, 011119B, 011119C, 011119D, 011119E,
011119F, 009119A, 009119B, 009119C, 009119D, 009119E, 009119F, 011079A, 011079B, 011079C,
011079D, 011079E, 013090A, 013090B, 013090C, 100020C, 100020D, 012090A, 012090B
Recall Number: D-251-1
Vintage Pharmaceuticals, Charlotte, NC
Vintage by letter on 3/21/01
FIRM INITIATED RECALL:
Q-Tuss Tablets - 110,538 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.