FDA Recall United States Ongoing Historical recordClass II
HU PRODUCTS
- Product
- Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4…
- Published
- March 17, 2021
- Distribution
- Multiple states
HU PRODUCTS Recall: may contain undeclared tree-nuts
United States
TerminatedClass II
- Company
- HU PRODUCTS
- Product
- Hu Vanilla Crunch Dark Chocolate bar
- Recall date
- May 17, 2023
- Terminated
- March 22, 2024
- Source
- FDA
Reason for recall
may contain undeclared tree-nuts
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Hu Vanilla Crunch Dark Chocolate bar | Not published in this source record | 363 cases - 52272 bars | L2343C best by 2024-12-09 UPC Codes: 850180006206 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0988-2023
- Event ID
- 92361
- Status
- Terminated
- Classification
- Class II
- Company
- HU PRODUCTS
- Product description
- Hu Vanilla Crunch Dark Chocolate bar
- Quantity
- 363 cases - 52272 bars
- Reason
- may contain undeclared tree-nuts
- Recall initiation date
- May 17, 2023
- Report date
- June 21, 2023
- Classification date
- Not published in this source record
- Termination date
- March 22, 2024
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- L2343C best by 2024-12-09 UPC Codes: 850180006206
- 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: HU PRODUCTS
Other recalls from HU PRODUCTS
FDA Recall United States Terminated Historical recordClass II
HU PRODUCTS
- Product
- Primary/Retail Package labeled in part: "Hu; CHOCOLATE-COVER…
- Published
- November 4, 2020
- Distribution
- Multiple states
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.
