FDA Recall United States Terminated Historical recordClass II
Giant Eagle, Inc.
- Product
- Market District Powerberry Mix covered in Dark Chocolate; N…
- Published
- November 15, 2017
- Distribution
- IN MD OH PA WV
Giant Eagle, Inc. Recall: On 10/30/2017, Giant Eagle received notice from their contract manufacturer to recall Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk in the dark chocolate. Giant Eagle product labels do carry the advisory statement "May Contain Milk".
United States
TerminatedClass II
- Company
- Giant Eagle, Inc.
- Product
- Market District Coffee Beans covered in Dark Chocolate; Net…
- Recall date
- October 30, 2017
- Terminated
- May 15, 2020
- Source
- FDA
Reason for recall
On 10/30/2017, Giant Eagle received notice from their contract manufacturer to recall Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk in the dark chocolate. Giant Eagle product labels do carry the advisory statement "May Contain Milk".
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Market District Coffee Beans covered in Dark Chocolate; Net Wt. 8 OZ.; Contains Soy; May Contain: Milk Manufactured in a plant that processes wheat, peanuts, tree nuts and eggs.; Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238-2809 | Not published in this source record | 6234 units | Coffee Beans UPC: 30034 09851; Almonds UPC: 30034 09852; Powerberry UPC: 30034 09857 |
Distribution
- IN MD OH PA WV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0353-2018
- Event ID
- 78423
- Status
- Terminated
- Classification
- Class II
- Company
- Giant Eagle, Inc.
- Product description
- Market District Coffee Beans covered in Dark Chocolate; Net Wt. 8 OZ.; Contains Soy; May Contain: Milk Manufactured in a plant that processes wheat, peanuts, tree nuts and eggs.; Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238-2809
- Quantity
- 6234 units
- Reason
- On 10/30/2017, Giant Eagle received notice from their contract manufacturer to recall Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk in the dark chocolate. Giant Eagle product labels do carry the advisory statement "May Contain Milk".
- Recall initiation date
- October 30, 2017
- Report date
- November 15, 2017
- Classification date
- Not published in this source record
- Termination date
- May 15, 2020
- Distribution pattern
- IN MD OH PA WV
- UPC, lot, and code information
- Coffee Beans UPC: 30034 09851; Almonds UPC: 30034 09852; Powerberry UPC: 30034 09857
- 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
Other products recalled under this same event
This recall shares FDA event ID 78423 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Giant Eagle, Inc.
- Product
- Market District Almonds covered in Dark Chocolate; Net Wt. 8…
- Published
- November 15, 2017
- Distribution
- IN MD OH PA WV
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-Large, Clam shell and Bowl, 9…
- 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-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 |
|---|---|
| Indiana | 1 |
| Maryland | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| West Virginia | 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.
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.
