Ben & Jerry's Pint Slices Chocolate Fudge Brownie 3 chocolate ice cream bars Net
Reason Unilever is voluntarily recalling a limited number of boxes of Ben & Jerry's Chocolate Fudge Brownie Pint Slices due to undeclared peanut.
Breyers¿ No Sugar Added Salted Caramel Swirl 1.5-quart recall
Recalled by Unilever United States, Inc. · Englewood Cliffs, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Unilever United States, Inc. is voluntarily recalling a limited number of tubs of Breyers¿ No Sugar Added Salted Caramel Swirl because they may inadvertently contain almonds, which are not listed as an ingredient on the label.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Breyers¿ No Sugar Added Salted Caramel Swirl 1.5-quart (1.41L) packaged in paperboard tubs Unilever, Englewood Cliffs, NJ 07632 USA Unit UPC: 7756738393. Product sold as 1.5-quart (1.41L) paperboard tubs, delivered to retailers in shrink wrap. Case UPC: 10077567383935
Quantity: 46,992 Consumer 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.
NOV2915GB
Where it was sold
Nationwide.
FDA's distribution note: Nationwide
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
- Unilever United States, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 16, 2015
- In FDA report of
- Apr 1, 2015
- Terminated
- Apr 3, 2017
- FDA recall number
- F-1584-2015 · event 70536
- Official record
- FDA enforcement report search
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