CLASS I Food recall · Reported 15 Sep 2021 · FDA Enforcement Report
Banoful Top Orange Biscuit recalled by KBF
KBF is recalling Banoful Top Orange Biscuit, distributed in 7 states. The recall was initiated on 30 Aug 2021 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1004-2021
- FDA event ID
- 88580
- Recalling firm
- KBF, Astoria, NY
- Brand
- Banoful Top
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 30 Aug 2021
- FDA classified
- 21 Sep 2021
- Reported
- 15 Sep 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Undeclared Milk
- Product category
- Citrus
Timeline
| 30 Aug 2021 | Recall initiated by company | |
| 15 Sep 2021 | Published in enforcement report | +16 days |
| 21 Sep 2021 | Classified by FDA | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
contains undeclared milk
Product as listed by the FDA
Banoful Top Orange Biscuit
Where it was distributed
New York, Maryland, Virginia, Pennsylvania, Connecticut, Massachusetts and Michigan
ConnecticutMassachusettsMarylandMichiganNew YorkPennsylvaniaVirginia
Questions about this recall
Is Banoful Top Orange Biscuit recalled?
Yes. KBF recalled Banoful Top Orange Biscuit on 30 Aug 2021. The recall is Class I and its status is Terminated. Recall number F-1004-2021.
Why was it recalled?
contains undeclared milk
Which lots are affected?
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.
Where was it sold?
New York, Maryland, Virginia, Pennsylvania, Connecticut, Massachusetts and Michigan
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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