Guest guest Posted September 24, 2003 Report Share Posted September 24, 2003 http://www.safetyalerts.com/recall/f/02.2/f0002766.htm SafetyAlerts June 25, 2003 Bristol-Myers Squibb Has Recalled Cholestyramine (SafetyAlerts) - The Food and Drug Administration (FDA) has released the following information. PRODUCT Cholestyramine for Oral Suspension, USP Powder, 4 grams cholestyramine resin, USP, per packet, 60 single dose packets, Apothecon. Recall # D-259-3. CODE Lot no. 1A32512 Exp. Date 2/29/2004. RECALLING FIRM/MANUFACTURER Recalling Firm: Bristol-Myers Squibb Company, New Brunswick, NJ, by letters on April 11, 2003. Manufacturing Firm: Bristol-Myers Squibb Company, Prinston, NJ. Firm initiated recall is ongoing. REASON Superpotent (6 month stability). VOLUME OF PRODUCT IN COMMERCE 2,011 ctns/60 packets ea. DISTRIBUTION Nationwide. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2003 Report Share Posted September 25, 2003 A lot of mold survivors got prescribed this as treatment. (It is the medication that used to be used for cholesteral problems.) I wanted people to know that it got recalled so they could talk to their doctors about different treatment. Quote Link to comment Share on other sites More sharing options...
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