Signature Kitchens Tuna Solid White
Reason Failed sensory analysis; decomposition.
SAFEWAY farms White Sliced Mushrooms***DISTRIBUTED BY SAFEWAY INC.***PLEASATON recall
Recalled by Safeway Inc · Pleasanton, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Champs 8 oz Sliced White Mushrooms are 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
"SAFEWAY farms White Sliced Mushrooms***DISTRIBUTED BY SAFEWAY INC.***PLEASATON, CA***PRODUCT OF CANADA***NET WT 8 OZ (227g)" UPC 0 21130 28443 6
Quantity: 230 cases from Auburn, WA DC; 50 cases from Spokane, WA DC
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 number 224S4189, UPC 0 21130 28443 6
Where it was sold
District of Columbia Idaho Montana Oregon Washington
FDA's distribution note: Auburn, WA DC and Spokane, WA DC - distributes to retail stores in OR, WA, ID and MT.
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
- Safeway Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 23, 2012
- In FDA report of
- Sep 12, 2012
- Terminated
- Sep 11, 2012
- FDA recall number
- F-2114-2012 · event 62995
- Official record
- FDA enforcement report search
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