Recall record at a glance
| Official record | F-1839-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Gift Services Inc Warehouse |
| Report date | Aug 29, 2018 |
| Recall initiation date | Jul 20, 2018 |
| Quantity | 38,079 packages |
| Location | Vancouver, WA, United States |
Official product description
Sherman Candy Caramels are individually wrapped in plastic and then sealed in a cardboard flexible carton. Each Sherman Candy Caramels contains 3 pieces inside and sold in the following gift baskets: Metropolitan Gourmet Gift Basket. Encore Gourmet Gift Basket. Toast of California Wine Basket. California Classic Gift Basket. The 5th Avenue Wine Gift Basket. Country Estate Gift Basket. Veuve Clicquot Tasting Gift Basket. No other products within these gift baskets are subject to recall. Sherman Candy Caramels are not sold separately. The Sherman Candy Caramels label is read in parts: "***SHERMAN CANDY CO. CARAMELS ***Ingredients: Milk Chocolate (sugar, milk, chocolate liquor, cocoa butter, soy lecithin [an emulsifier], vanilla), Dark Chocolate (sugar, chocolate liquor, cocoa butter, soy lecithin [an emulsifier], vanilla), Coconut Oil, White Chocolate (sugar, cocoa butter, whole milk powder, soy lecithin (an emulsifier), nautral vanilla flavor), Butter Oil, Natural Flavor, Soy Lecithin, Salt ***CONTAINS: Coconut, Milk, Soy ***".
Why the product was recalled
Sherman Candy Caramels product is recalled due to undeclared pecans, walnuts, almonds and/or peanuts.
Distribution information
sold directly to consumers nationwide through two online retail platforms GiftTree.com and 1stopflorists.com
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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.