FDA Recall United States TerminatedTerminated: March 7, 2024Historical recordClass I
FreshPoint Dallas
- Product
- Whole cantaloupe 3ct and 6ct
- Published
- December 13, 2023
- Distribution
- Institutions, medical facilities and dir…
FreshPoint Dallas Recall: Potential Foreign Material
United States
TerminatedClass II
- Company
- FreshPoint Dallas
- Product
- FC TOMATOES ROMA DICED 3/8" 1/5#; FC TOMATOES ROMA DICED 3/8…
- Recall date
- October 20, 2020
- Terminated
- December 2, 2020
- Source
- FDA
Reason for recall
Potential Foreign Material
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| FC TOMATOES ROMA DICED 3/8" 1/5#; FC TOMATOES ROMA DICED 3/8" 4/5#, and FC TOMATOES ROMA DICED 3/8" 2/5# all packaged in white plastic trays with heat seal lid, packed inside a cardboard box | Not published in this source record | 142 cases | LOT CODE: 7420286 |
Distribution
- Texas and Kansas
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0119-2021
- Event ID
- 86683
- Status
- Terminated
- Classification
- Class II
- Company
- FreshPoint Dallas
- Product description
- FC TOMATOES ROMA DICED 3/8" 1/5#; FC TOMATOES ROMA DICED 3/8" 4/5#, and FC TOMATOES ROMA DICED 3/8" 2/5# all packaged in white plastic trays with heat seal lid, packed inside a cardboard box
- Quantity
- 142 cases
- Reason
- Potential Foreign Material
- Recall initiation date
- October 20, 2020
- Report date
- November 25, 2020
- Classification date
- Not published in this source record
- Termination date
- December 2, 2020
- Distribution pattern
- Texas and Kansas
- UPC, lot, and code information
- LOT CODE: 7420286
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: FreshPoint Dallas
Other recalls from FreshPoint Dallas
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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.
