CLASS II Food recall · Reported 20 Sep 2023 · FDA Enforcement Report
US Foods: Peanut Butter Toffee Bar unit size recalled by Killer Brownie
Killer Brownie is recalling US Foods: Peanut Butter Toffee Bar unit size, distributed in Illinois. The recall was initiated on 31 Aug 2023 and the FDA has classified it as Class II.
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-1512-2023
- FDA event ID
- 92998
- Recalling firm
- Killer Brownie, Miamisburg, OH
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 31 Aug 2023
- FDA classified
- 13 Sep 2023
- Reported
- 20 Sep 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Foreign Material
- Product category
- Ready Meals
Timeline
| 31 Aug 2023 | Recall initiated by company | |
| 13 Sep 2023 | Classified by FDA | +13 days |
| 20 Sep 2023 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Foreign Material - Plastic
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
US Foods: Peanut Butter Toffee Bar, 3.4oz unit size, packaged in flow wrap, 24 packages per case
Where it was distributed
Distributed to IL
Questions about this recall
Why was it recalled?
Foreign Material - Plastic
Which lots are affected?
Lot No. 203KB650PR3, 203KB650MX3 Product No. 1020435
Where was it sold?
Distributed to IL
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.