Recall record at a glance
| Official record | F-1581-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Chocolate By Design, Inc. |
| Report date | Apr 1, 2015 |
| Recall initiation date | Feb 12, 2015 |
| Quantity | 10 boxes (24 pops per box) |
| Location | Ronkonkoma, NY, United States |
Official product description
Assorted Milk Chocolate Royal Icing Pops sold as Assorted Character Icing Pops, Christmas Icing Pops, and Triple Heart Icing Pops, 24 pops per box. The Milk Chocolate Icing Pops are made to order and sold in unmarked bulk boxes. Each Milk Chocolate Icing Pop is individually wrapped for retail sale in 2 oz. clear cellophane with a curl ribbon closure.
Why the product was recalled
The products contain undeclared egg and FD&C colors Yellow 5 or 6, Red 3 or 40, and/or Blue 1 from the royal icing component used on the finished pops.
Distribution information
New York, New Jersey and Virginia
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: Telephone.
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.