← FDA ENFORCEMENT
F-1317-2024Class I

Danisco USA Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Danisco USA Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-06-12
Distribution
US: AZ, CA, CO, FL, IA, ID, IL, IN, KS, KY, MI, MN, MO, NE, NJ, NY, OH, OK, PA, TN, TX, UT, VA, WI; Canada, and Mexico
Firm state
KS
Product quantity
13608 kg
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential Salmonella Contamination

Product description

ASC 2138 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag

Code / lot info

Lot numbers: 1204612405; 1204612406; 1204612407; 1204612408; 1204612409; 1204612410; 1204612411; 1204612412; 1204612413; 1204612414; 1204612415; 1204612416; 1204612417; 1204612418; 1204612419; 1204623758; 1204623759; 1204623760; 1204623761; 1204623762; 1204623763; 1204623764; 1204623765; 1204623766; 1204623768; 1204623769; 1204623770; 1204623771; 1204623772; 1204623774

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →