Recall record at a glance
| Official record | F-0289-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Klosterman Baking Company |
| Report date | Jan 25, 2023 |
| Recall initiation date | Dec 18, 2022 |
| Quantity | 109,343 (total) |
| Location | Indianapolis, IN, United States |
Official product description
Breads: Yellow product 1444 Clear Bag Loaf 1 32 oz. Yellow product 1675 Clear Bag Loaf 1 24 oz. Yellow product 3139 Clear Bag Buns 12 60 g Yellow product 3148 Clear Bag Buns 12 60 g Yellow product 3385 Clear Bag Buns 12 85 g Yellow product 3396 Clear Bag Buns 12 85 g Yellow product 3531 Clear Bag Buns 12 80 g Yellow product 2590 Clear Bag Buns 12 92 g Yellow product 3592 Clear Film Buns 20 92 g Yellow product 3644 Clear Bag Buns 12 100 g Yellow product 8090 Clear Bag Rolls 12 1.2 oz.
Why the product was recalled
Products held under insanitary conditions
Distribution information
IN, OH, TN
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.