Product is a liquid dietary supplement packaged in white plastic bottles with a shrink wrap sleeve label. The

Recall map → All recalls → F-0594-2013

Product is a liquid dietary supplement packaged in white plastic bottles with a shrink wrap sleeve label. The product comes in 3 sizes, 2 oz, 16oz. and 33.8oz. The product label reads in part: "Fast Absorbing Liquid 1-OZ A DAYWELLESSEDigestive 3-in-1 Health Soluble Fiber Prebiotics Aloe Vera Promotes Gentle Regularity Supports Health Bacteria Balances Stomach AcidityIsomaltooligosaccharides (Prebiotic Fiber),GalactooligosaccharidesOther Ingredients: Purified WaterManufactured By: Botanical Laboratories, Inc. Ferndale, WA 98248 USA***" Botanical Laboratories Inc · reported 2012-11-07

Terminated This recall has been closed out by the agency.

Reason for recall: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonella by the raw ingredient supplier.
Classification: Class I
Recall initiated: 2012-06-04
Reported by the agency: 2012-11-07
Closed out (terminated): 2013-04-03
Recalling firm: Botanical Laboratories Inc
Ferndale, WA
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): Nationwide to retailers (80%) and consumers (direct and sample 20 %) - approximate
States we parsed from that text: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WYour expansion
The agency wrote a broader phrase; these state names are ours, not theirs. Parse method nationwide, confidence high.
Food category: Dietary supplements Prepared meals & entreesderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-0594-2013

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.