Recall record at a glance
| Official record | F-2083-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Schulze & Burch Biscuit Co |
| Report date | Sep 14, 2016 |
| Recall initiation date | Jun 1, 2016 |
| Quantity | 64,955 cases (or) 779,460 cartons, 12 Cartons per case |
| Location | Chicago, IL, United States |
Official product description
Aldi's Millville protein chew bars, peanut, dark chocolate & almond packaged 5 bars per box in a yellow and brown box with brown and white lettering.
Why the product was recalled
A supplier of one of the ingredients in the protein chewy bars informed firm of Listeria Monocytogenes positive.
Distribution information
The product was shipped to Aldi Inc. , 1200 Kirk Road, Batavia, IL 60510 from there it is further shipped to distribution centers andd then to Aldi stores. no product was distributed to foreign firms.
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: Telephone.
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.