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AMS Health Sciences

2 recall records on file.

2014

2 records

Class ITerminatedRecall F-0462-2015

Product description

Saba Shark Cartilage Complex Dietary Supplement, 500 mg, 60 Capsules, Distributed by Saba 711 NE 39th Street, Oklahoma City, OK 73105

Reason for recall

The product is being recalled due to the potential presence of Salmonella.

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Event ID
69498
Code info
Lot number 416349, 08/16
Product quantity
2,014 bottles
Distribution pattern
Nationwide throughout the US and in Canada
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type
Food
Recalling firm location
711 NE 39th St, N/A, Oklahoma City, OK, United States
Recall initiation date
10/15/2014
Center classification date
11/05/2014
Termination date
02/09/2016
Class IITerminatedRecall F-0018-2015

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.

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Event ID
67701
Code info
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
Product quantity
1,021,350 - 2 pack samples; 8,595,450 - 60 ct bottle
Distribution pattern
OK, CO,
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Other
Product type
Food
Recalling firm location
711 NE 39th St, Oklahoma City, OK, United States
Recall initiation date
02/26/2014
Center classification date
10/09/2014
Termination date
09/22/2016