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FDA recall record

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

Recall F-1115-2024Class IITerminatedFebruary 29, 2024

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of September 12, 2024. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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

Reason

Potential contamination with Clostridium botulinum

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

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

Code information listed by FDA

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

Distribution and firm information

Recalling firm listed by FDA: AJI MORI SAUCE CORP

Firm location listed by FDA: Los Angeles, CA, United States

Distribution reported by FDA: 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.

Product quantity listed by FDA: 78 bottles

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.