Ferrara Candy Company Recall: Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
United States
TerminatedClass III
- Company
- Ferrara Candy Company
- Product
- Ferrara Candy Company assorted candy Heart Box, including La…
- Recall date
- February 18, 2021
- Terminated
- September 1, 2021
- Source
- FDA
Reason for recall
Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Ferrara Candy Company assorted candy Heart Box, including Laffy Taffy, Nerds, and SweeTarts candies. 10 retail units per wholesale case. Package UPC 0 41420 04965 1 | Not published in this source record | 3832 cases | All product distributed prior to 2/18/2021 |
Distribution
- Nationwide retail
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0336-2021
- Event ID
- 87338
- Status
- Terminated
- Classification
- Class III
- Company
- Ferrara Candy Company
- Product description
- Ferrara Candy Company assorted candy Heart Box, including Laffy Taffy, Nerds, and SweeTarts candies. 10 retail units per wholesale case. Package UPC 0 41420 04965 1
- Quantity
- 3832 cases
- Reason
- Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
- Recall initiation date
- February 18, 2021
- Report date
- March 10, 2021
- Classification date
- Not published in this source record
- Termination date
- September 1, 2021
- Distribution pattern
- Nationwide retail
- UPC, lot, and code information
- All product distributed prior to 2/18/2021
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Ferrara Candy Company
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
