FCF Item 403953 HEB Poblano Caesar Dressing recall

Recalled by Reser's Fine Foods, Inc. · Beaverton, OR, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished wholesale and retail RTE products.

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

FCF Item 403953, HEB Poblano Caesar Dressing, 12oz. glass bottle, 6 bottles per case. UPC 41220 94807

Quantity: 2495 cases

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.

Lot 166609-001, Use By 1/14/2024 Lot 168402-001, Use By 2/9/2024 Lot 169789-001, Use By 3/4/2024 Lot 171446-001, Use By 3/31/2024

Where it was sold

California Connecticut Florida Idaho Illinois Maryland Montana New Jersey Nevada Oregon Pennsylvania South Dakota Texas Utah Virginia Washington

FDA's distribution note: Distributed in CA, CT, FL, ID, IL, MD, MT, NJ, NV, OR, PA, SD, TX, UT, VA, and WA.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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: Reser's Fine Foods, Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Feb 6, 2024
In FDA report of: Mar 27, 2024
Terminated: Jul 5, 2024
FDA recall number: F-1089-2024 · event 93961
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class I · High risk Terminated Listeria Feb 6, 2024