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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
The firm initiated a voluntary recall of Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., packed in a stand up pouch, due to mislabeling. The label declared cream, milk, and eggs, which were not part of the original formula. The label lacked the following ingredients: Spices, Artificial Flavors, Garlic Powder, Onion Powder, Dextrose, Worcestershire Sauce, Corn Syrup, Salt, Carmel Color, Sugar, Tamarind, Natural Flavor, Malic Acid, Olive Oil, Molasses Sucralose, Bourbon Whiskey, Sulfites & Celery Seeds.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., 6/case, packed in a stand-up pouch. | Not published in this source record | 4730.24 lbs. | Meijer Honey Vanilla Bourbon Pecans Manufactured 11/1/2017-12/5/2017, Codes: 09 6340, 09 6322Z, 09 6306, 09 6312, 09 6322Y |
Responsible company: Meijer, Inc #816 - Grand River Packaging
FDA Recall United States TerminatedTerminated: August 12, 2025Historical recordClass II
FDA Recall United States TerminatedTerminated: July 10, 2018Historical recordClass II
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 |
|---|---|
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Michigan | 1 |
| Ohio | 1 |
| Wisconsin | 1 |
| 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.
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This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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Retrieved by Public Health Trace:
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.
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.
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