Unilever United States, Inc. FDA recall records
The FDA has published 6 food recall enforcement records naming Unilever United States, Inc. between 2013 and 2017, covering 6 separate recall events. The firm is recorded in New Jersey. Data last updated 2 September 2026.

- Records of 29,386
- 6
- Share of all recalls
- 0%
- Class I of 6
- 3
- Reported between
- 2013 to 2017
What these records are
Every record on this page was published by the FDA in the openFDA food enforcement database. 6 records cover 6 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.
3 of these records are Class I, 3 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.
What was recalled for
A single record can name more than one hazard, so these counts overlap.
By year
Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.
Where the recalling firms are
The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.
Most recently reported
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2017-07-12 | Ben & Jerry's Pint Slices Chocolate Fudge Brownie 3 chocolate ice cream bars Net 9 FL OZ. UPC code 076840657940 | Unilever United States, Inc. | Unilever is voluntarily recalling a limited number of boxes of Ben & Jerry's Chocolate Fudge Brownie Pint Slices due to undeclared peanut. | Class II |
| 2016-12-28 | Ben & Jerrys Brownie Batter Core Ice Cream One Pint (473 mL). Case UPC- 10076840529879 Consumer UPC - 7684052987 Paper carton 8 units per shrink-wrapped case Frozen | Unilever United States, Inc. | Certain pints of Ben & Jerrys Brownie Batter Core Ice Cream may contain soft plastic pieces. | Class II |
| 2015-04-15 | Talenti Gelato & Sorbetto, 1 pt. (473 mL) in clear plastic jars with best by date 5/19/2016, UPC 8685200024 | Unilever United States, Inc. | Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a limited number of jars of Talenti Gelato & Sorbetto Sea Salt Carmel Gelato because they may inadvertently contain peanuts (as peanut butter) which are not listed as an ingredient on the label. | Class I |
| 2015-04-01 | 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 | Unilever United States, Inc. | 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. | Class I |
| 2014-04-09 | Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs, NJ 07632 USA UPC 077567121301 | Unilever United States, Inc. | Unilever United States, Inc. is voluntarily recalling a limited number of 20-count boxes of Popsicle brand Orange, Cherry and Grape flavored ice pops because they may have been inadvertently exposed to milk, which is not listed as an ingredient on the label. | Class I |
| 2013-01-23 | Knorr Pasta Sides Cheesy Bacon Macaroni Net Wt. 3.8 oz, (107 g) Unilever Englewood Cliffs, NJ 07632 USA Made in Canada from domestic and imported ingredients Case SCC 10041000082488 UPC 4100008248 | Unilever United States, Inc. | Knorr Pasta Sides Cheesy Bacon Macaroni may contain soy as a different product mix was inadvertently packaged in the Cheesy Bacon Macaroni pouch. | Class II |
Questions
- How many FDA recalls has Unilever United States, Inc. had?
- The FDA has published 6 food recall enforcement records naming Unilever United States, Inc. between 2013 and 2017. Those records cover 6 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
- Does a high recall count mean a firm is unsafe?
- Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.
A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.