FDA Recall United States Terminated Historical recordClass II
Grace Kennedy Foods USA LLC
- Product
- La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Distribute…
- Published
- April 5, 2017
- Distribution
- Nationwide
Grace Kennedy Foods USA LLC Recall: Presence of plastic in bagged frozen peppers and onions.
United States
TerminatedClass II
- Company
- Grace Kennedy Foods USA LLC
- Product
- La Fe Brand Frozen Peppers and Onions 16 oz bags.
- Recall date
- March 22, 2021
- Terminated
- March 25, 2022
- Source
- FDA
Reason for recall
Presence of plastic in bagged frozen peppers and onions.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| La Fe Brand Frozen Peppers and Onions 16 oz bags. | Not published in this source record | 187 CASES (12 bags per case) | LOT # KR043021, Batch # K10605 |
Distribution
- Distributed to retail stores in CT
- DE
- MA
- NJ
- NY
- and PA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0362-2021
- Event ID
- 87573
- Status
- Terminated
- Classification
- Class II
- Company
- Grace Kennedy Foods USA LLC
- Product description
- La Fe Brand Frozen Peppers and Onions 16 oz bags.
- Quantity
- 187 CASES (12 bags per case)
- Reason
- Presence of plastic in bagged frozen peppers and onions.
- Recall initiation date
- March 22, 2021
- Report date
- April 7, 2021
- Classification date
- Not published in this source record
- Termination date
- March 25, 2022
- Distribution pattern
- Distributed to retail stores in CT, DE, MA, NJ, NY, and PA
- UPC, lot, and code information
- LOT # KR043021, Batch # K10605
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Grace Kennedy Foods USA LLC
Other recalls from Grace Kennedy Foods USA LLC
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 |
|---|---|
| Connecticut | 1 |
| Delaware | 1 |
| Massachusetts | 1 |
| New Jersey | 1 |
| New York | 1 |
| Pennsylvania | 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.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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