Class IITerminatedVoluntary: Firm initiated
Dollar General Corporation: food recall H-0499-2025
Dollar General Corporation of Goodlettsville, TN recalled Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069,… Reason: Potential presence of glass pieces. The FDA listed it as Class II in its Enforcement Report dated Aug 20, 2025; distribution: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, Wyoming.
Record status as published: Terminated (terminated Apr 6, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069, Distributed By Old East Main Co. 100 Mission Ridge Goodlettsville, TN 37072
- Product quantity
- 84,240 units
- Reason for recall
- Potential presence of glass pieces
- Codes, lots and dates on the package
- BEST BEFORE: 12/12/26 Lot: 5163 BEST BEFORE: 12/13/26 Lot: 5164 BEST BEFORE: 12/14/26 Lot: 5165
- Distribution pattern
- AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
- Recalling firm
- Dollar General Corporation, Goodlettsville, TN
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jul 27, 2025 |
| Classified by the FDA | Aug 14, 2025 |
| Published in the Enforcement Report | Aug 20, 2025 |
| Terminated | Apr 6, 2026 |
Other recalls by Dollar General Corporation
- H-0418-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0417-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0416-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0415-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0414-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0413-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0412-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0411-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0410-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
- H-0409-2025 · Aug 13, 2025 · Class II — Temperature abuse due to temperature excursion in one shipping trailer
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0499-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.