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June 21, 2001

Pharmacist FormulaÆ Maximum Strength Non-Aspirin Sinus Caplets Recalled

Carson, CA (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Leiner Health Products, Inc. has recalled certain Pharmacist FormulaÆ Maximum Strength Non-Aspirin Sinus Caplets because of misbranding. The Blister strips incorrectly list Chlorpheniramine Maleate as an ingredient.

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

Pharmacist FormulaÆ Maximum Strength Non-Aspirin Sinus Caplets, (Acetaminophen 500mg/Pseudophedrine HCL 30mg), units of 24.

Recall # D-231-1.

LOT NO. OPB1174.

Leiner Health Products, Inc., Carson, CA.

Manufacturer, by letter on 4/19/01. Firm-initiated recall ongoing.



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 June 21, 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!

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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.