FDA Recall United States TerminatedTerminated: March 8, 2022Historical recordClass I
Onions 52
- Product
- 12 count per 2 lb. mesh sacks with UPC 033383 601014 Medium…
- Published
- December 8, 2021
- Distribution
- Nationwide
Onions 52 Recall: Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico. - F-0230-2022
United States
TerminatedClass I
- Company
- Onions 52
- Product
- 40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico -…
- Recall date
- October 21, 2021
- Terminated
- March 8, 2022
- Source
- FDA
Reason for recall
Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico - Label Carzalia Valley Produce, Distributed by Carzalia Valley Produce, Columbus, NM. UPC 00815222010023 Imported from Chihuahua, Mexico, sourced from ProSource and shipped from July 1, 2021 through August 25, 2021. Store in cool dry place off the ground. | 00815222010023 | 200 - 40# Cartons | 40# CTN, 194, 1176114, 23862060 40# CTN, 194, 1176116, 23862060 40# CTN, 202, 1176111, 23860999 40# CTN, 202, 1176112, 23860999 40# CTN, 202, 1176113, 23860999 40# CTN, 202, 1176115, 23860999 40# CTN Pack date, lot codes, customer PO# |
Distribution
- Nationwide
- NE
- TN
- TX.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0230-2022
- Event ID
- 88994
- Status
- Terminated
- Classification
- Class I
- Company
- Onions 52
- Product description
- 40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico - Label Carzalia Valley Produce, Distributed by Carzalia Valley Produce, Columbus, NM. UPC 00815222010023 Imported from Chihuahua, Mexico, sourced from ProSource and shipped from July 1, 2021 through August 25, 2021. Store in cool dry place off the ground.
- Quantity
- 200 - 40# Cartons
- Reason
- Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico.
- Recall initiation date
- October 21, 2021
- Report date
- December 8, 2021
- Classification date
- Not published in this source record
- Termination date
- March 8, 2022
- Distribution pattern
- Nationwide, NE, TN, TX.
- UPC, lot, and code information
- UPC 00815222010023; 40# CTN, 194, 1176114, 23862060 40# CTN, 194, 1176116, 23862060 40# CTN, 202, 1176111, 23860999 40# CTN, 202, 1176112, 23860999 40# CTN, 202, 1176113, 23860999 40# CTN, 202, 1176115, 23860999 40# CTN Pack date, lot codes, customer PO#
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- 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 88994 with 2 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: March 8, 2022Historical recordClass I
Onions 52
- Product
- 5# (LB) Ctn (box) Jumbo Red Onions, Product of Mexico - Labe…
- Published
- December 8, 2021
- Distribution
- Nationwide
Responsible company: Onions 52
Other recalls from Onions 52
FDA Recall United States TerminatedTerminated: March 8, 2022Historical recordClass I
Onions 52
- Product
- 12 count per 2 lb. mesh sacks with UPC 033383 601014 Medium…
- Published
- December 8, 2021
- Distribution
- Nationwide
FDA Recall United States TerminatedTerminated: March 8, 2022Historical recordClass I
Onions 52
- Product
- 5# (LB) Ctn (box) Jumbo Red Onions, Product of Mexico - Labe…
- Published
- December 8, 2021
- Distribution
- Nationwide
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 |
|---|---|
| Nebraska | 1 |
| Tennessee | 1 |
| Texas | 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.
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. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of March 8, 2022.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.