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SafetyAlerts
March 7, 2001

Anso Comfort™ Capsules Recalled

Arcadia, CA (SafetyAlerts) - The Food and Drug Administration (FDA) has posted additional information concerning the Anso Comfort™ recall previously annouced by the California State Department of Health.   The product contains the undeclared prescription drug-chlordiazdepoxide.

This is recall has been classified Class II by FDA.

PRODUCT
(OTC) Anso Comfort™ Capsules, Extract of Hainanensis Merr Leaf, 200 mg, 60 capsules per bottle.

Recall #D-100-1.

CODE:
Lot 0H0041, Sept 2003 and Lot 9422, Exp 7-2002.

MANUFACTURER:
Numeridian, Inc., Arcadia, CA.

RECALLED BY:
Manufacturer, by letter on 2/5/01. Firm-initiated recall ongoing.

DISTRIBUTION:
AK, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, PA, RI, SC, TN, TX, UT, VA, WA, and WI.
Foreign distribution was to China (Shanghai), and Canada (BC and Ontario).

QUANTITY:
Lot OH0041, 6420 bottles; Lot 9422, unknown.

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 March 7, 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.