Advanced Fresh Concepts Sushi Shrimp Recall: Vibrio Parahaemolyticus Risk
Advanced Fresh Concepts recalls sushi shrimp from Thailand due to Vibrio parahaem: a foodborne pathogen causing stomach illness. Consumers should check lot numbers and contact the company for details.
Lower-risk recall
Firm testing found Vibrio parahaemolyticus in cooked butterfly shrimp from Thailand.
Contact the company
What happened, in plain English
Advanced Fresh Concepts is recalling sushi shrimp from Thailand that tested positive for Vibrio parahaemolyticus, a bacteria that can cause stomach illness. This recall is due to potential food safety risks from contaminated shrimp. Read more at govinfonow.com/recall/15802-advanced-fresh-concepts-sushi-shrimp-recall-vibrio-parahaemolyticus-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/15802-advanced-fresh-concepts-sushi-shrimp-recall-vibrio-parahaemolyticus-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0875-2020
Cite this page
“Advanced Fresh Concepts Sushi Shrimp Recall: Vibrio Parahaemolyticus Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15802-advanced-fresh-concepts-sushi-shrimp-recall-vibrio-parahaemolyticus-risk. Based on FDA recall #F-0875-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0875-2020%22&limit=1).
Why it’s dangerous
Vibrio parahaemolyticus is a bacteria that can cause stomach illness, including diarrhea and vomiting. The shrimp was found to contain this bacteria after firm testing from Thailand.
Who’s affected
Anyone who purchased the sushi shrimp from Thailand. Those with compromised immune systems may be at higher risk.
How to tell if you have this one
Check for the lot number 2019.10.02 on the shrimp packaging. The product is sold in trays of 20 individual shrimp, each weighing 0.498 pounds.
- Brand
Advanced Fresh Concepts- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot number 2019.10.02 on the shrimp packaging.
Where it went and when
Where it was distributed
Distributed in 40 states.
FDA distribution: “AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NH, NM, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, New Hampshire, New Mexico, New York, North Carolina, North Dakota, Ohio, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wyoming.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0875-2020 (March 12, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0875-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.