Recall record at a glance
| Official record | F-1888-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Seattle Pops |
| Report date | Apr 15, 2015 |
| Recall initiation date | Dec 23, 2014 |
| Quantity | 23 pops |
| Location | Seattle, WA, United States |
Official product description
Arroz con Leche Frozen Pops, 4.0 fl oz. frozen pop is individually packaged in a sealed plastic bag; 24 pops/case. Product is labeled in part, "***rice, cinnamon, vanilla, cream, milk, skim milk powder, non-gmo cane sugar, less than 0.4% stabilizer (carob bean gum, guar gum, soy lecithin, carrageenan)***Seattle Pops PO Box 31285 Seattle, WA 98103***". No UPC code.
Why the product was recalled
Ice Cream Bars/Pops are recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain an ice cream based ingredient that was manufactured and recalled by Snoqualmie Gourmet Ice Cream, Inc.
Distribution information
Product was distributed in Washington state.
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: E-Mail.
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.