CLASS II Drug recall · Reported 27 Feb 2019 · FDA Enforcement Report
tubby todd Bath Co, 100% Natural Dream Cream, Shea Butter and Mint recalled
Mariposa Labs is recalling tubby todd Bath Co, 100% Natural Dream Cream, Shea Butter and Mint, distributed in California. The recall was initiated on 12 Nov 2015 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0510-2019
- FDA event ID
- 82112
- Recalling firm
- Mariposa Labs, Boise, ID
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Nov 2015
- FDA classified
- 19 Feb 2019
- Reported
- 27 Feb 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Mold
- Drug class
- Creams, Ointments & Gels
Timeline
| 12 Nov 2015 | Recall initiated by company | |
| 19 Feb 2019 | Classified by FDA | +1195 days |
| 27 Feb 2019 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold.
Product as listed by the FDA
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.
Where it was distributed
Distributed in California
Questions about this recall
Why was it recalled?
Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold.
Which lots are affected?
Lot#: 5589, Exp. 08/2017
Where was it sold?
Distributed in California
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Mariposa Labs
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | NorthStar Arthritis Relief Cream recalled by Mariposa Labs | Mariposa Labs | Sterility | ID |