Severity
Critical
FDA Food recall · Reported November 7, 2012
Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonella by the raw ingredient supplier.
Botanical Laboratories Inc recalled Product is a liquid dietary supplement packaged in white plastic bottles with a shrink wr… - a critical-severity action.
Product is a liquid dietary supplement packaged in white plastic bottles with a shrink wr… was recalled by Botanical Laboratories Inc in November 7, 2012. Reason: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonel…. Check the official notice for the remedy. Verify recall #F-0594-2013 with the FDA Food before acting.
The recall
Botanical Laboratories Inc issued this critical-severity FDA Food recall-Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonel….
Sourced from official FDA Food enforcement records. Verify recall #F-0594-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0594-2013) was formally reported on November 7, 2012, with the manufacturer initiating the action on June 4, 2012. It is classified under Critical severity (Class I), with a current status of Terminated. Botanical Laboratories Inc is listed as the recalling firm, operating out of Ferndale, WA. Federal records list the affected scope as 2 oz.- 6,509,16oz - 10,846 and 33.8oz - 21,093 units (minus some quality and production retains).
The documented reason for this recall is: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonella by the raw ingredient supplier. Distribution data in the federal record shows the product reached: Nationwide to retailers (80%) and consumers (direct and sample 20 %) - approximate. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
2 oz.- 6,509,16oz - 10,846 and 33.8oz - 21,093 units (minus some quality and production retains)
Related Recalls
6
6 from same agency
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 DAY***WELLESSE***Digestive 3-in-1 Health Soluble Fiber Prebiotics Aloe Vera Promotes Gentle Regularity Supports Health Bacteria Balances Stomach Acidity***Isomaltooligosaccharides (Prebiotic Fiber),***Galactooligosaccharides***Other Ingredients: Purified Water***Manufactured By: Botanical Laboratories, Inc. Ferndale, WA 98248 USA***"
Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonella by the raw ingredient supplier.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-0594-2013 |
| Date reported | November 7, 2012 |
| Date initiated | June 4, 2012 |
| Recalling firm | Botanical Laboratories Inc |
| Firm location | Ferndale, WA |
| Affected scope | 2 oz.- 6,509,16oz - 10,846 and 33.8oz - 21,093 units (minus some quality and production retains) |
| Distribution | Nationwide to retailers (80%) and consumers (direct and sample 20 %) - approximate |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 7, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.