FDA Recall United States Ongoing2026 recordClass II
Lidl US TRADING
- Product
- ERIDANOUS GREEK STYLE Shortbread Cookies with apricot fillin…
- Published
- September 2, 2026
- Distribution
- Product was shipped to the following sta…
Lidl US TRADING Recall: Lidl US, LLC has initiated a recall of Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes per case and 3 popcorn bags per box. Best by/Lot Codes: JUL192021N2, JUL232021N2, AUG182021N2 because the raw ingredient supplier for the popcorn has initiated a recall due to foreign material. - F-0074-2021
United States
TerminatedClass II
- Company
- Lidl US TRADING
- Product
- Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes p…
- Recall date
- September 9, 2020
- Terminated
- February 2, 2022
- Source
- FDA
Reason for recall
Lidl US, LLC has initiated a recall of Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes per case and 3 popcorn bags per box. Best by/Lot Codes: JUL192021N2, JUL232021N2, AUG182021N2 because the raw ingredient supplier for the popcorn has initiated a recall due to foreign material.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes per case and 3 popcorn bags per box . | Not published in this source record | 3,782 retail units | Article Number (Internal Use): 216367 Retail Unit UPC: 20741570 Best by/Lot Codes: - JUL192021N2 - JUL232021N2 - AUG182021N2 |
Distribution
- States were stores are located: VA
- MD
- NC
- NY
- MD
- PA
- NJ and DE
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0074-2021
- Event ID
- 86489
- Status
- Terminated
- Classification
- Class II
- Company
- Lidl US TRADING
- Product description
- Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes per case and 3 popcorn bags per box .
- Quantity
- 3,782 retail units
- Reason
- Lidl US, LLC has initiated a recall of Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes per case and 3 popcorn bags per box. Best by/Lot Codes: JUL192021N2, JUL232021N2, AUG182021N2 because the raw ingredient supplier for the popcorn has initiated a recall due to foreign material.
- Recall initiation date
- September 9, 2020
- Report date
- November 11, 2020
- Classification date
- Not published in this source record
- Termination date
- February 2, 2022
- Distribution pattern
- States were stores are located: VA, MD, NC, NY, MD, PA, NJ and DE
- UPC, lot, and code information
- Article Number (Internal Use): 216367 Retail Unit UPC: 20741570 Best by/Lot Codes: - JUL192021N2 - JUL232021N2 - AUG182021N2
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Lidl US TRADING
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- Product
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- Distribution
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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 |
|---|---|
| Virginia | 1 |
| Maryland | 1 |
| North Carolina | 1 |
| New York | 1 |
| Pennsylvania | 1 |
| New Jersey | 1 |
| Delaware | 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 II mean?
FDA classifies this recall as Class II. 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
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How to interpret this historical record
This record is preserved as published by FDA, as of February 2, 2022.
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.
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