FDA Recall United States Terminated Historical recordClass I
Betty Lou's Inc
- Product
- Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, C…
- Published
- August 16, 2023
- Distribution
- Nationwide
Betty Lou's Inc Recall: Undeclared Sesame
United States
TerminatedClass II
- Company
- Betty Lou's Inc
- Product
- Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.…
- Recall date
- October 9, 2023
- Terminated
- December 27, 2023
- Source
- FDA
Reason for recall
Undeclared Sesame
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UPC 0 16073 00213 1. There are 12 packages per display box (box UPC 0 16073 00223 0). The label allergens contains statement declares Milk, Peanut, Tree Nuts (Almond, Cashew, Coconut, Hazelnut). | Not published in this source record | 5,197 bars | BB 05APR24 hh:mm F6 0053 The code breaks down as: BB 05APR24: Best by Day, Month, Year hh:mm hour and minute of packaging F6 is packaging line identifier. 005: Julian Date of Manufactured Date 3: Last digit of Manufactured Year 0053: Manufactured on January 5th, 2023 |
Distribution
- Distributed in AL
- AR
- AZ
- CA
- CO
- CT
- FL
- GA
- IA
- ID
- IL
- KY
- MA
- MI
- MT
- NV
- NY
- OH
- OK
- OR
- PA
- TN
- TX
- WA
- WI
- and WY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0301-2024
- Event ID
- 93205
- Status
- Terminated
- Classification
- Class II
- Company
- Betty Lou's Inc
- Product description
- Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UPC 0 16073 00213 1. There are 12 packages per display box (box UPC 0 16073 00223 0). The label allergens contains statement declares Milk, Peanut, Tree Nuts (Almond, Cashew, Coconut, Hazelnut).
- Quantity
- 5,197 bars
- Reason
- Undeclared Sesame
- Recall initiation date
- October 9, 2023
- Report date
- November 1, 2023
- Classification date
- Not published in this source record
- Termination date
- December 27, 2023
- Distribution pattern
- Distributed in AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, KY, MA, MI, MT, NV, NY, OH, OK, OR, PA, TN, TX, WA, WI, and WY.
- UPC, lot, and code information
- BB 05APR24 hh:mm F6 0053 The code breaks down as: BB 05APR24: Best by Day, Month, Year hh:mm hour and minute of packaging F6 is packaging line identifier. 005: Julian Date of Manufactured Date 3: Last digit of Manufactured Year 0053: Manufactured on January 5th, 2023
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Betty Lou's Inc
Other recalls from Betty Lou's Inc
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Massachusetts | 1 |
| Michigan | 1 |
| Montana | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
