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SafetyAlerts
July 11, 2001

Zenith Goldline Pharmaceuticals Recalls Methocarbamol and Aspirin Tablets

Northvale, NJ (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Zenith Goldline  Pharmaceuticals of Northvale, NJ is recalling certain lot(s) of Methocarbamol and Aspirin Tablets because of superpotency-(ASPIRIN COMPONE NT).

Methocarbamol is used to treat acute, painfulconditions, and is in a class of drugs known as centrally acting skeletalmuscle relaxants.

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

PRODUCT AND CODE:
Methocarbamol and Aspirin Tablets 400mg/325mg; Rx Zenith
Goldline, NDC#0172-2813-60

Lot Numbers:
2813-098-- 6/2001
2813--99V--5/2002
2813-100V--6/2002

RECALL NUMBER:
D-242-1.

REASON:
SUPER-POTENCY-(ASPIRIN COMPONE NT)

MANUFACTURER/RECALLING FIRM:
Zenith Goldline Pharmaceuticals Northvale, NJ

RECALLED BY:
The recalling firm sent a product Recall Letter dated 1/10/01 was mailed to all direct accounts.

FIRM INITIATED RECALL:
Ongoing

DISTRIBUTION:
Nationwide

QUANTITY:
9235 x 100 tablet bottles.

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

 
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.