Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported October 15, 2014
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105
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 anal…
The recall
Ams Health Sciences issued this moderate-severity FDA Food recall — Product called SABA ACE (Appetite Control Energy) that was manufactured prior to September 2013 was found to ….
- Moderate
- severity level
- Class II
- classification
- October 15, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0018-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0018-2015) was formally reported on October 15, 2014, with the manufacturer initiating the action on February 26, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Ams Health Sciences is listed as the recalling firm, operating out of Oklahoma City, OK. Federal records list the affected scope as 1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle.
The documented reason for this recall is: 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 prod… Distribution data in the federal record shows the product reached: OK, CO,. 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, 5 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.
Dietary Supplements recalls over time
Where this recall sits in its category — 711 dietary supplements recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Affected scope
1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle
Related Recalls
6
5 from same agency
Product description
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0018-2015 |
| Date reported | October 15, 2014 |
| Date initiated | February 26, 2014 |
| Recalling firm | Ams Health Sciences |
| Firm location | Oklahoma City, OK |
| Affected scope | 1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle |
| Distribution | OK, CO, |
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.
- Check the recall number (F-0018-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting — recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105. Recalled by Ams Health Sciences. Units affected: 1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle.
Why was this product 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 agency issued this recall? ▼
This recall was issued by the FDA Food on October 15, 2014. Severity: Moderate. Recall number: F-0018-2015.
Where was the recalled product distributed? ▼
Distribution: OK, CO,.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0018-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported October 15, 2014.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.