CLASS II Food recall · Reported 15 Oct 2014 · FDA Enforcement Report
saba; ACE; Appetite Control Energy; 052234; 07/2015 recalled
AMS Health Sciences is recalling saba; ACE; Appetite Control Energy; 052234; 07/2015, distributed in Colorado, Oklahoma. The recall was initiated on 26 Feb 2014 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-0018-2015
- FDA event ID
- 67701
- Recalling firm
- AMS Health Sciences, Oklahoma City, OK
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Feb 2014
- FDA classified
- 9 Oct 2014
- Reported
- 15 Oct 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Other
- Reason category
- Hidden Drug Ingredients
- Product category
- Weight Loss Supplements
Timeline
| 26 Feb 2014 | Recall initiated by company | |
| 9 Oct 2014 | Classified by FDA | +225 days |
| 15 Oct 2014 | 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 called SABA ACE (Appetite Control Energy) that was manufactured prior to September 2013 was found to have DMAA (1,3-Dimethylpentylamine) based on label and laboratory analysis. the DMAA was removed when the product was reformulated in September 2013.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105
Where it was distributed
OK, CO,
Questions about this recall
Why was it recalled?
Product called SABA ACE (Appetite Control Energy) that was manufactured prior to September 2013 was found to have DMAA (1,3-Dimethylpentylamine) based on label and laboratory analysis. the DMAA was removed when the product was reformulated in September 2013.
Which lots are affected?
Lot Numbers: 81721, 81722, 101022, 61327, 61328, 61329, 31424, 31422, 31423, 40926, 40925, 33125, 31421, 31324, 30922, 30923, 30924, 31322, 31323, 31321, 12428, 30925, 12426, 21325, 12521,112214, 112216, 52231, 52232, 20634, 31832, 31833, 40833, 31831, 31838, 33033, 330353, 33031, 33034, 33032, 31834, 31837, 31835, 31836, 20634, 20635, 21837, 21834, 21835, 21836, 31537, 11131, 20633, 121024, 121025, 121026, 121027, 21831, 36000250, 110524, 110525, 101024, 33126, 61325, 981723, 101023, 110523
Where was it sold?
OK, CO,
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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