Saba Shark Cartilage Complex Dietary Supplement
Reason The product is being recalled due to the potential presence of Salmonella.
saba; ACE Appetite Control Energy recall
Recalled by AMS Health Sciences · Oklahoma City, OK, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was 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.
The label gives no warning, so buyers cannot know about dangerous interactions with medicines they already take. All hidden drug ingredients recalls.
What was recalled
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105
Quantity: 1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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 it was sold
Colorado Oklahoma
FDA's distribution note: OK, CO,
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- AMS Health Sciences
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 26, 2014
- In FDA report of
- Oct 15, 2014
- Terminated
- Sep 22, 2016
- FDA recall number
- F-0018-2015 · event 67701
- Official record
- FDA enforcement report search