Reser's Fine Foods recalls HEB Cilantro Cotija Dressing due to potential Listeria monocytogenes contamination in repackaged products. Affected items have specific lot numbers and use-by dates.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.
Reser's Fine Foods is recalling HEB Cilantro Cotija Dressing products that were repackaged into finished products. This could pose a Listeria risk, which can cause serious illness if consumed.
Listeria monocytogenes is a bacteria that can cause serious illness, including meningitis and sepsis, especially in pregnant women, newborns, and immunocompromised individuals. The recalled dressing was repackaged into finished products, increasing the risk of contamination.
People who bought the HEB Cilantro Cotija Dressing in 12oz glass bottles, 6 per case, with specific lot numbers and use-by dates are affected. Those who have consumed the product are at risk of Listeria infection.
Check for the 12oz glass bottle with 6 bottles per case. Look for lot numbers 166604-001 (use by 1/13/2024), 168400-001 (use by 2/9/2024), 169787-001 (use by 3/4/2024), or 171443-001 (use by 3/30/2024).
Identify the lot number and use-by date on the bottle to confirm if it's affected.
The product is not safe to consume if it's a recalled lot. Affected items have been repackaged and may contain Listeria monocytogenes.
Check the lot number and use-by date. If it matches the recalled lots, stop using it and contact HEB for instructions.
Do not consume the recalled dressing. Proper food handling and storage can reduce the risk of Listeria infection.
We’ve drafted a message you can send Reser's to request your refund or repair — edit it as you like.
Subject: Recall F-1088-2024 — Reser's Reser's Hello, I own a Reser's that is covered by recall F-1088-2024 from Reser's. 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.
