Recall record at a glance
| Official record | F-0624-2021 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | American Pop Corn Co |
| Report date | Jun 2, 2021 |
| Recall initiation date | May 12, 2021 |
| Quantity | 286 cases |
| Location | Sioux City, IA, United States |
Official product description
Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa
Why the product was recalled
Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk.
Distribution information
Distributed to distribution centers in CA, IA, KS, NE, and UT for final retail store distribution to potentially AZ, CA, CO, ID, IA, KS, MN, MO, MT, NE, NV, OR, SD, UT, WI and WY.
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.