Yeast Extract Ajirex in 15 kg PE bag in carton box
FINDARECALL QUICK READ
What this record tells you
This FDA record concerns Yeast Extract Ajirex in 15 kg PE bag in carton box and names Mitsubishi International Food Ingredients, Inc. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.
- Firm: Mitsubishi International Food Ingredients, Inc.
- Classification: Class II
- Status: Terminated
- Recall date: 2021-11-29
Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.
FDA public announcements can appear before an enforcement report is classified, so an empty classification does not mean the notice is unimportant.
Product Description & Identification
Yeast Extract Ajirex in 15 kg PE bag in carton box
Reason for Recall / Hazard Identified
Potential Salmonella contamination.
How to Check Whether Your Product Matches
A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.
- Confirm the full product and brand or recalling-firm name.
- Compare package size, color, flavor, model, style, or configuration when listed.
- Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
- Review the recall date and distribution information without assuming every seller is listed.
- Open the official FDA source below and follow its current instructions.
If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.
Consumer Action Recorded in the Source
Distribution & Affected States
Products were distributed to the following states: GA, IL, PA, & TX. *Firm has been notified by GFS that they did use some of the recalled product in production. GFS is in HAFE3 and has been notified of this situation.
Verify With the Issuing Agency
This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.
Open FDA Source Record →Record Transparency
- Issuing agency
- FDA
- Source ID
- F-0285-2022
- Indexed update
- 2026-08-09 21:59:13 UTC
- Official source
- Open issuing-agency record