Pico De Gallo
Reason Potential contamination with Salmonella.
Aji Mori***chillimami Sauce***umami Bomb*** recall
Recalled by Aji Mori Sauce CORP · Los Angeles, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Potential contamination with Clostridium botulinum
Pathogen: Botulism
Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
AJI MORI***CHILLIMAMI SAUCE***UMAMI BOMB***NET WT. 250ml. Packaged in a LDPE bottle. Refrigerate after opening.
Quantity: 78 bottles
Food: Sauces, dips & dressings
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
California Florida Illinois Massachusetts New Jersey Nevada New York Texas Virginia
FDA's distribution note: 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.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Aji Mori Sauce CORP
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 29, 2024
- In FDA report of
- Apr 10, 2024
- Terminated
- Sep 12, 2024
- FDA recall number
- F-1115-2024 · event 94176
- Official record
- FDA enforcement report search
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