FDA Recall United States Terminated Historical recordClass I
Triple B Corporation
- Product
- Charlies Produce Anchorage, YELLOW Peeled Onions, Jumbo, Rea…
- Published
- September 9, 2020
- Distribution
- distributed in AK only.
Triple B Corporation Recall: Charlies Produce peeled onions products are recalled due to a potential contamination with Salmonella Newport.
United States
TerminatedClass I
- Company
- Triple B Corporation
- Product
- Charlie s Produce Anchorage, RED Peeled Onions, Jumbo, Ready…
- Recall date
- August 5, 2020
- Terminated
- September 28, 2020
- Source
- FDA
Reason for recall
Charlies Produce peeled onions products are recalled due to a potential contamination with Salmonella Newport.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Charlie s Produce Anchorage, RED Peeled Onions, Jumbo, Ready To Eat (RTE), keep refrigerated. Shelf-life: packing date plus 6 days, packed in corrugated cardboard box. Net. wt. 20 lbs., no UPC. Product was peeled and packaged by Charlie s Produce 9401 King St., Anchorage, AK 99515. | Not published in this source record | 52 cases (20 lbs. per case). | Pack Dates: 07/21/20 to 8/3/20. Use by Dates: pack date plus 6 days. |
Distribution
- distributed in AK only.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1336-2020
- Event ID
- 86183
- Status
- Terminated
- Classification
- Class I
- Company
- Triple B Corporation
- Product description
- Charlie s Produce Anchorage, RED Peeled Onions, Jumbo, Ready To Eat (RTE), keep refrigerated. Shelf-life: packing date plus 6 days, packed in corrugated cardboard box. Net. wt. 20 lbs., no UPC. Product was peeled and packaged by Charlie s Produce 9401 King St., Anchorage, AK 99515.
- Quantity
- 52 cases (20 lbs. per case).
- Reason
- Charlies Produce peeled onions products are recalled due to a potential contamination with Salmonella Newport.
- Recall initiation date
- August 5, 2020
- Report date
- September 9, 2020
- Classification date
- Not published in this source record
- Termination date
- September 28, 2020
- Distribution pattern
- distributed in AK only.
- UPC, lot, and code information
- Pack Dates: 07/21/20 to 8/3/20. Use by Dates: pack date plus 6 days.
- 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
Other products recalled under this same event
This recall shares FDA event ID 86183 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
Triple B Corporation
- Product
- Charlies Produce Anchorage, WHITE Peeled Onions, Jumbo, Read…
- Published
- September 9, 2020
- Distribution
- distributed in AK only.
Responsible company: Triple B Corporation
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Triple B Corporation
- Product
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- Published
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- Distribution
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FDA Recall United States Terminated Historical recordClass II
Triple B Corporation
- Product
- Charlie's brand perishable and refrigerated Spinach Salad Wi…
- Published
- September 14, 2022
- Distribution
- Distributed in Idaho, Montana, Oregon, a…
FDA Recall United States Terminated Historical recordClass I
Triple B Corporation
- Product
- Charlies Produce Anchorage, YELLOW Peeled Onions, Jumbo, Rea…
- Published
- September 9, 2020
- Distribution
- distributed in AK only.
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 |
|---|---|
| Alaska | 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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
