Recall record at a glance
| Official record | F-1650-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Kellogg Company |
| Report date | Jun 27, 2018 |
| Recall initiation date | Jun 14, 2018 |
| Quantity | 1,145,030 Cases |
| Location | Battle Creek, MI, United States |
Official product description
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
Why the product was recalled
Kellogg North America initiated a voluntary recall of Kellogg s Honey Smacks, 15.3 oz. and 23 oz., due to potential contamination with Salmonella.
Distribution information
Domestic: Alabama Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii, Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakokta South Dakota Tennessee Texas Utah Virginia Washington West Virginia Wisconsin Wyoming Foreign:Aruba Bahamas Bayamon Frenc.Polynesia Guam Guatemala Haiti Nether.Antill. Northern Mariana Isl Panama Saint George Tortola US Virgin Islands Mexico Costa Rica Military: Alabama California Florida Hawaii Indiana Maryland Mississippi Montana Oklahoma Pennsylvania Texas Virginia
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.