KBF INC Recall: contains undeclared milk - F-1004-2021
United States
TerminatedClass I
- Company
- KBF INC
- Product
- Banoful Top Orange Biscuit
- Recall date
- August 30, 2021
- Terminated
- March 17, 2023
- Source
- FDA
Reason for recall
contains undeclared milk
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Banoful Top Orange Biscuit | Not published in this source record | 99 cartons | Batch code KBF/05 MFG 15.06.2020 EXP 14.06.2022, Batch code KBF/07 MFG 20.07/2020 EXP 19.07.2022 Batch code KBF/11 MFG 15.10.2020 EXP 14.10.2022 The product UPC code is 8 941114 001427. |
Distribution
- New York
- Maryland
- Virginia
- Pennsylvania
- Connecticut
- Massachusetts and Michigan
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1004-2021
- Event ID
- 88580
- Status
- Terminated
- Classification
- Class I
- Company
- KBF INC
- Product description
- Banoful Top Orange Biscuit
- Quantity
- 99 cartons
- Reason
- contains undeclared milk
- Recall initiation date
- August 30, 2021
- Report date
- September 15, 2021
- Classification date
- Not published in this source record
- Termination date
- March 17, 2023
- Distribution pattern
- New York, Maryland, Virginia, Pennsylvania, Connecticut, Massachusetts and Michigan
- UPC, lot, and code information
- Batch code KBF/05 MFG 15.06.2020 EXP 14.06.2022, Batch code KBF/07 MFG 20.07/2020 EXP 19.07.2022 Batch code KBF/11 MFG 15.10.2020 EXP 14.10.2022 The product UPC code is 8 941114 001427.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- N/A
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: KBF INC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of March 17, 2023.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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