Whole Foods Vegan Buffalo Chicken Bites
Reason The firm is recalling the products listed below because it is mislabeled. Products labeled as Vegan Buffalo Chicken Bites are in fact Vegan Sonoma Chicken Salad. The label fails to declare Pecans.
Whole Foods Market PB & J Parfait Made With Greek Yogurt recall
Recalled by Sunneen Health Foods, LLC · Allentown, PA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Sunneel Health Foods received a call from their customer indicating some of their Vegan Match Cocoa Parfaits were misbranded as PB & J Parfaits. The ingredient statement failed to declare Soy, Almonds and Coconut allergens.
Undeclared allergens: Tree nuts 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
Whole Foods Market PB & J Parfait Made With Greek Yogurt; Net Wt 8 OZ.;
Quantity: 30 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.
Expiration date 7/13/17
Where it was sold
New Jersey New York
FDA's distribution note: NJ, NY
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 tree nuts, 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
- Sunneen Health Foods, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 8, 2017
- In FDA report of
- Aug 16, 2017
- Terminated
- Jan 26, 2018
- FDA recall number
- F-3350-2017 · event 77730
- Official record
- FDA enforcement report search