← FDA ENFORCEMENT
F-1115-2024Class II

AJI MORI SAUCE CORP

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
AJI MORI SAUCE CORP
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-04-10
Distribution
Products were distributed direct to consumers in CA, TX, IL, FL, NV, NY, NJ, VA, MA. The firm distributed products to consumers at their retail location and to customers who purchased product from their website, www.ajimorisauce.com.
Firm state
CA
Product quantity
78 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential contamination with Clostridium botulinum

Product description

AJI MORI***CHILLIMAMI SAUCE***UMAMI BOMB***NET WT. 250ml. Packaged in a LDPE bottle. Refrigerate after opening.

Code / lot info

Batch Numbers: 231001; 240101; 231002; 240102; 231003; 240103; 231004; 240104; 231101; 240105; 231102; 240106; 231103; 240201; 231104; 240202; 231201; 240203; 231202; 240204; 231203; 231204. Product code: 86001056573, Expiration Date: Oct 1, 2024

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 →