American Pop Corn Co Recall: Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk. - F-0624-2021
United States
TerminatedClass I
- Company
- American Pop Corn Co
- Product
- Xtra Butter Microwave Popcorn bags packaged in cardboard box…
- Recall date
- May 12, 2021
- Terminated
- July 8, 2021
- Source
- FDA
Reason for recall
Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 286 cases | 01/25/2022 1025 (time code) 3&4 |
Distribution
- 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.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0624-2021
- Event ID
- 87935
- Status
- Terminated
- Classification
- Class I
- Company
- American Pop Corn Co
- 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
- Quantity
- 286 cases
- Reason
- Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk.
- Recall initiation date
- May 12, 2021
- Report date
- June 2, 2021
- Classification date
- Not published in this source record
- Termination date
- July 8, 2021
- Distribution pattern
- 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.
- UPC, lot, and code information
- 01/25/2022 1025 (time code) 3&4
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: American Pop Corn Co
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| California | 1 |
| Iowa | 1 |
| Kansas | 1 |
| Nebraska | 1 |
| Utah | 1 |
| Arizona | 1 |
| Colorado | 1 |
| Idaho | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| Nevada | 1 |
| Oregon | 1 |
| South Dakota | 1 |
| Wisconsin | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of July 8, 2021.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.