Dole brand Sliced Mushrooms recall
Recalled by Oakshire Mushroom Sales, Llc · Kennett Square, PA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product recalled due to potential contamination of Listeria monocytogenes.
Pathogen: Listeria
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
Dole brand Sliced Mushrooms, Net Wt. 8 OZ. (227G), UPC: 0 33383 67600 5, in a plastic container over-wrapped with plastic film. Labeled in part: Dole Sliced Mushrooms, Distributed by Oakshire Mushroom Sales, LLC under license Kennett Square, PA 19348 1-866-355-2077, Product of Canada
Quantity: 160 cases w/ 12 - 8 ounce containers per case.
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.
"33 6" - represents the week of year plus one day of week. Code is etched on label near "Distributed by" text.
Where it was sold
FDA's distribution note: Distributed to a single account (Albertson's).
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
- Oakshire Mushroom Sales, Llc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 23, 2012
- In FDA report of
- Oct 10, 2012
- Terminated
- Nov 2, 2012
- FDA recall number
- F-0012-2013 · event 62997
- Official record
- FDA enforcement report search