Recall record at a glance
| Official record | F-1846-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Armour Eckrich Meats LLC |
| Report date | Aug 3, 2016 |
| Recall initiation date | Jun 15, 2016 |
| Quantity | 5403 cases / 18 packages per case |
| Location | Lisle, IL, United States |
Official product description
Armour Snackmaker Keebler Animals Crackers, Chocolate Icing with Natural and Artificial Flavors, Plain Icing which are packaged in 2.7oz packages; Unit UPC code 2781500240 . There are 18 packages to a case, Case SKU 2781500240. The responsible firm name on the label is Armour-Eckrich Meats LLC, Cincinnati, OH 45240.
Why the product was recalled
Product contains an ingredient which is being recalled from their supplier due to the potential of low levels of peanut residue.
Distribution information
Cases were distributed nationwide. No government or military distribution.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
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.