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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 67701

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 26, 2014
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
AMS Health Sciences

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105

F-0018-2015
Recall number
F-0018-2015
Initiated
February 26, 2014
Classification
Class II
Status
Terminated
Recalling firm
AMS Health Sciences
Quantity
1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

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

Distribution pattern

OK, CO,