simply to go Strawberry Yogurt Parfaits
Reason Product contains undeclared soy lecithin and brown sugar syrup.
simply to go Blueberry Yogurt Parfaits recall
Recalled by Sodexo Operations, LLC · Billerica, MA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains undeclared soy lecithin and brown sugar syrup.
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
simply to go Blueberry Yogurt Parfaits, 8.53oz, UPC 477088156552 and 477088150550; packaged in plastic cups
Quantity: 23,059 plastic cups/units
Food: Milk & dairy Berries
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.
UPC: 477088156552 and 477088150550 Sell By Dates up to and including 05/08/2023
Where it was sold
Massachusetts New Hampshire Rhode Island
FDA's distribution note: MA, NH, RI
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Sodexo Operations, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 8, 2023
- In FDA report of
- Jun 14, 2023
- Terminated
- Jul 6, 2023
- FDA recall number
- F-0972-2023 · event 92295
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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