Wiers Farm Organic Cucumber packaged into recall

Recalled by Wiers Farm Inc · Willard, OH, United States

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

Why it was recalled

Listeria monocyotgenes contamination

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

Wiers Farm - Organic Cucumber packaged into 2 count trays - cases dependent on customer

Quantity: 113 cases

Food: Cucumbers

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 No 240705, 240706, 240707, 240708, 240709, 240710, 240711, 240712

Where it was sold

Connecticut Delaware Illinois Indiana Kentucky Maryland Maine Michigan Missouri North Carolina New Jersey New York Ohio Pennsylvania Rhode Island Tennessee Virginia West Virginia

FDA's distribution note: CT, DE, IL, IN, KY, ME, MD, MI, MO, NJ, NY, NC, OH, PA, RI, TN, VA, WV

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: Wiers Farm Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Jul 11, 2024
In FDA report of: Aug 14, 2024
Terminated: Aug 23, 2024
FDA recall number: F-1682-2024 · event 94998
Official record: FDA enforcement report search

Also recalled with it (26 more products)

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

Class I · High risk Terminated Listeria Jul 11, 2024