Severity
Moderate
FDA Drug recall · Reported February 27, 2019
Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold.
Mariposa Labs LLC recalled tubby todd Bath Co, 100% NATURAL DREAM CREAM, Shea Butter and Mint, 3.5 FL OZ 99G, Distri… - a moderate-severity action.
tubby todd Bath Co, 100% NATURAL DREAM CREAM, Shea Butter and Mint, 3.5 FL OZ 99G, Distri… was recalled by Mariposa Labs LLC in February 27, 2019. Reason: Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be ou…. Check the official notice for the remedy. Verify recall #D-0510-2019 with the FDA Drug before acting.
The recall
Mariposa Labs LLC issued this moderate-severity FDA Drug recall-Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be ou….
Sourced from official FDA Drug enforcement records. Verify recall #D-0510-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0510-2019) was formally reported on February 27, 2019, with the manufacturer initiating the action on November 12, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Mariposa Labs LLC is listed as the recalling firm, operating out of Boise, ID. Federal records list the affected scope as 1654 jars.
The documented reason for this recall is: Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold. Distribution data in the federal record shows the product reached: Distributed in California. 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, 3 from FDA Drug - 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 - 1,371 cosmetics & personal care recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
1654 jars
Related Recalls
6
3 from same agency
tubby todd Bath Co, 100% NATURAL DREAM CREAM, Shea Butter and Mint, 3.5 FL OZ 99G, Distributed by: Tubby Todd Bath Co. Vista, CA 920, (619) 894-6560.
Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0510-2019 |
| Date reported | February 27, 2019 |
| Date initiated | November 12, 2015 |
| Recalling firm | Mariposa Labs LLC |
| Firm location | Boise, ID |
| Affected scope | 1654 jars |
| Distribution | Distributed in California |
Profile values are sourced directly from the official FDA Drug 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 Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Same archive severity grade (Moderate), closest by report date among other firms and states.
Same product category, closest by report date among other firms and states (deduped against the severity set).
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 Drug, reported February 27, 2019. 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 August 2026.