Evolve Double Chocolate Plant-Based Protein Shake
Reason undeclared soy
Evolve Vanilla Bean Plant-Based Protein Shake recall
Recalled by Pepsico Inc · Purchase, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
undeclared soy
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
Evolve Vanilla Bean Plant-Based Protein Shake, 11oz "Tetra Pak" carton, sold 4 cartons per retail unit. UPC on retail 4 pack: 876063007870 Packed 3 retail four packs per wholesale case.
Quantity: 14830 cases
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.
Best Before: DEC 30 21 Best Before: JAN 25 22 MFG Date: 12-30-20 MFG Date: 01-25-21 Production code: DEC 30 21 ###### XXXXXU12300 Production code: JAN 25 22 ###### XXXXXU01251
Where it was sold
Nationwide.
FDA's distribution note: Nationwide through retailers, eCommerce, professional and collegiate athletic organizations.
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
- Pepsico Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 29, 2021
- In FDA report of
- May 26, 2021
- Terminated
- Feb 1, 2022
- FDA recall number
- F-0538-2021 · event 87835
- 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.
Other recalls by Pepsico Inc
Class II · Moderate risk Terminated
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Reason Product was mislabeled. Can labeled as regular Mug contains Mug Zero Sugar
Schweppes ZERO SUGAR GINGER ALE CAFFIENE FREE
Reason During an internal investigation the firm discovered that product labeled as Zero Sugar contains full sugar product.
Lipton Diet Green Tea Citrus
Reason Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)