Recall record at a glance
| Official record | F-1475-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Unilever |
| Report date | Jun 26, 2019 |
| Recall initiation date | Apr 15, 2019 |
| Quantity | 18,638 (total) |
| Location | Englewood Cliffs, NJ, United States |
Official product description
Ben & Jerry s Coconut Seven Layer Bar Bulk . The product is sold in a tub containing 2.4 gallons .
Why the product was recalled
Unilever is voluntarily recalling a limited quantity of Ben & Jerry s Coconut Seven Layer Bar bulk and Ben & Jerry s Chunky Monkey pints, because product contains undeclared tree nuts, brazil nuts, hazelnuts and almonds that are not declared in the ingredient list or allergy information list. The affected Ben & Jerry s Coconut Seven Layer Bar bulk product is sold in a tub containing 2.4 gallons with a Consumer UPC of 076840104246 and best by date of SEP1520BJ4. The affected Ben & Jerry s Chunky Monkey pint is sold in a pint tub (473 mL) with a Consumer UPC of 076840100354 and best by dates of AUG2820BH2, AUG2920BH2, or AUG3020BH2.
Distribution information
Thru out the United States.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.