CLASS II Food recall · Reported 18 May 2016 · FDA Enforcement Report
SeeLessO'Me Diet and Weight Management Tea recalled by Nuwati Herbals
Nuwati Herbals is recalling SeeLessO'Me Diet and Weight Management Tea, distributed nationwide in the US. The recall was initiated on 15 Mar 2016 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1331-2016
- FDA event ID
- 73554
- Recalling firm
- Nuwati Herbals, Saint Charles, MO
- Brand
- SeeLessO'Me Diet
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 15 Mar 2016
- FDA classified
- 12 May 2016
- Reported
- 18 May 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Soy
- Product category
- Herbal Supplements
Timeline
| 15 Mar 2016 | Recall initiated by company | |
| 12 May 2016 | Classified by FDA | +58 days |
| 18 May 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains undeclared soy.
Product as listed by the FDA
Nuwati Herbals SeeLessO'Me Diet and Weight Management Tea packaged in two different size amber glass jars with Net Wt 3 oz. or Net Wt 6 oz. The responsible name on the label is Nuwati Herbals Inc., House Springs, MO.
Where it was distributed
Nationwide.
Questions about this recall
Why was it recalled?
Product contains undeclared soy.
Which lots are affected?
all codes from 2011 through 2016
Where was it sold?
Nationwide.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
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.
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