Food FDA Class II Terminated Foreign material
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
Dollar General Corporation Published Aug 20, 2025
Risk level
Class IIMay cause a temporary or reversible health problem; slight chance of serious harm.
Severity score 50/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- Do not eat, serve, or sell the affected product.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact Dollar General Corporation or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Potential presence of glass pieces
Hazards
Glass · primary
Affected products (1)
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
84,240 units
Lot codes: 5163, 5164, 5165
Code info: BEST BEFORE: 12/12/26 Lot: 5163 BEST BEFORE: 12/13/26 Lot: 5164 BEST BEFORE: 12/14/26 Lot: 5165
Affected areas
AlabamaArizonaArkansasCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaOhioOklahomaOregonPennsylvaniaRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahVermontVirginiaWashingtonWest VirginiaWisconsinWyoming
Timeline
- InitiatedJul 27, 2025
- PublishedAug 20, 2025
- TerminatedApr 6, 2026
- Recall number
- H-0499-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.