FDA Recall United States Terminated Historical recordClass I
Giant Eagle, Inc.
- Product
- Smoked Mozzarella Penne Salad-Large, Clam shell and Bowl, 9…
- Published
- October 29, 2025
- Distribution
- The adulterated product was sold in the…
Giant Eagle, Inc. Recall: Giant Eagle supplier SunOpta has informed Giant Eagle of the expansion of their sunflower kernel recall due to possible Listeria monocytogenes contamination. Giant Eagle repacked the sunflower kernels under the Market District label, which were sold in the bulk section of 12 of its Market District stores. Giant Eagle has expanded their recall to include all lots of sunflower seeds
United States
TerminatedClass I
- Company
- Giant Eagle, Inc.
- Product
- Sunflower Seeds, PLU# 65167; various weights; various sell…
- Recall date
- May 3, 2016
- Terminated
- August 15, 2017
- Source
- FDA
Reason for recall
Giant Eagle supplier SunOpta has informed Giant Eagle of the expansion of their sunflower kernel recall due to possible Listeria monocytogenes contamination. Giant Eagle repacked the sunflower kernels under the Market District label, which were sold in the bulk section of 12 of its Market District stores. Giant Eagle has expanded their recall to include all lots of sunflower seeds
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sunflower Seeds, PLU# 65167; various weights; various sell by dates; Market District; Distributed by Giant Eagle, Pittsburgh, PA 15238 | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- PA
- OH
- IN
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1836-2016
- Status
- Terminated
- Classification
- Class I
- Company
- Giant Eagle, Inc.
- Product description
- Sunflower Seeds, PLU# 65167; various weights; various sell by dates; Market District; Distributed by Giant Eagle, Pittsburgh, PA 15238
- Quantity
- Not published in this source record
- Reason
- Giant Eagle supplier SunOpta has informed Giant Eagle of the expansion of their sunflower kernel recall due to possible Listeria monocytogenes contamination. Giant Eagle repacked the sunflower kernels under the Market District label, which were sold in the bulk section of 12 of its Market District stores. Giant Eagle has expanded their recall to include all lots of sunflower seeds
- Recall initiation date
- May 3, 2016
- Report date
- August 3, 2016
- Classification date
- Not published in this source record
- Termination date
- August 15, 2017
- Distribution pattern
- PA, OH, IN
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Giant Eagle, Inc.
Other recalls from Giant Eagle, Inc.
FDA Recall United States Terminated Historical recordClass I
Giant Eagle, Inc.
- Product
- Smoked Mozzarella Penne Salad-Small, Clam shell and Bowl, 4…
- Published
- October 29, 2025
- Distribution
- The adulterated product was sold in the…
FDA Recall United States Terminated Historical recordClass I
Giant Eagle, Inc.
- Product
- Smoked Mozzarella Penne Salad, bulk, UPC 256616000000
- Published
- October 29, 2025
- Distribution
- The adulterated product was sold in the…
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 |
|---|---|
| Pennsylvania | 1 |
| Ohio | 1 |
| Indiana | 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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
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.
