JFE FRANCHISING INC recalls Diced Pepper Tri-Blend and Fajita Mix products due to Listeria monocytogenes contamination. Consumers should avoid these items as they pose a risk of serious illness.
Listeria monocytogenes
JFE FRANCHISING INC is recalling several pepper and spice blends that may contain Listeria monocytogenes, a bacteria that can cause serious foodborne illness. This recall affects products sold through their restaurants and retail locations.
Listeria monocytogenes is a bacteria that can grow in refrigerated foods and cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. This recall is for products that may have been contaminated during manufacturing.
Anyone who purchased JFE's Diced Pepper Tri-Blend, Diced Pepper w/ White Onion, or Fajita Mix products from their restaurants or retail stores. People with weakened immune systems are at higher risk for severe illness.
Check for product codes: 639123880024 (8 oz Diced Pepper Tri-Blend), 639123880048 (7 oz Diced Pepper w/ White Onion), 639123880406 (11 oz Fajita Mix, Hot), and 639123880390 (11 oz Fajita Mix, Mild). Products were sold with a sell-by date through July 26, 2024.
Discard any recalled products immediately as they may contain harmful bacteria.
The recalled products include Diced Pepper Tri-Blend (8 oz, code 639123880024), Diced Pepper w/ White Onion (7 oz, code 639123880048), Fajita Mix (Hot, 11 oz, code 639123880406), and Fajita Mix (Mild, 11 oz, code 639123880390).
Check the product code on the container. Recalled products have codes 639123880024, 639123880048, 639123880406, or 639123880390 and were sold with a sell-by date through July 26, 2024.
The recall does not specify a remedy; consumers should discard the products immediately.
We’ve drafted a message you can send JFE to request your refund or repair — edit it as you like.
Subject: Recall F-1763-2024 — JFE JFE Hello, I own a JFE that is covered by recall F-1763-2024 from JFE. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
