Locatelli Pecorino Romano Cheese Grated
Reason Product may be contaminated with Listeria monocytogenes.
Wegmans Bakery Mini Muffins APPLE CINNAMON recall
Recalled by Wegmans Food Markets · Rochester, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The Apple Cinnamon Mini Muffins contain undeclared soy, a known allergen.
Undeclared allergen: Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Wegmans Bakery Mini Muffins APPLE CINNAMON, NET WT 14 OZ (397g) , UPC 77890 18951 --- Baked By Wegmans Food Markets Inc., Rochester, NY 14603
Quantity: 4,327 units
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.
All date codes up to and including "Best if used by 9/24/13"
Where it was sold
Massachusetts Maryland New Jersey New York Pennsylvania Virginia
FDA's distribution note: New York, Pennsylvania, New Jersey, Maryland, Virginia, and Massachusetts.
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. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. 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
- Wegmans Food Markets
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 19, 2013
- In FDA report of
- Oct 23, 2013
- Terminated
- Oct 17, 2013
- FDA recall number
- F-0002-2014 · event 66324
- Official record
- FDA enforcement report search
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