Highline Mushrooms Sliced recall
Recalled by Ciolino Wholesale Produce, Inc. · Temperance, MI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
On 8/13/12, Highline Mushrooms, of Ontario Canada, voluntarily recalled lots of sliced, white mushrooms that may be contaminated with Listeria monocytogenes. Ciolino Wholesale Produce, Inc. received a shipment of the mushrooms and initiated their own voluntary recall upon receiving notice from Highline Mushrooms.
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
Highline Mushrooms Sliced, white mushrooms 8 oz.
Quantity: 7cs-84/8 oz. packages, or a total of 588/8 oz
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.
Size: 8 oz. UPC: 7 71163 00005 2 Lot #: L410805 plus 4-digit time code Date Code: Best Before 12AU15
Where it was sold
Michigan Ohio
FDA's distribution note: MI and OH distribution only. Retail only.
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
- Ciolino Wholesale Produce, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 17, 2012
- In FDA report of
- Sep 5, 2012
- Terminated
- Nov 8, 2012
- FDA recall number
- F-2094-2012 · event 62374
- Official record
- FDA enforcement report search