40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico - Label Carzalia Valley Produce, Distributed by Carzalia Valle
Summary
The FDA issued a Class I for 40# (LB) Ctn (box) Jumbo Yellow Onions, Product of Mexico - Label Carzalia Valle by Onions 52. Reason: Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico..
Details
Source
Food Recall
External ID
F-0230-2022
Action Date
2021-12-08
Status
Terminated
Category
food
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.
Lot/Code Info: 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#
Quantity Affected: 200 - 40# Cartons
Reason for Recall
Voluntary recall due to possible contamination with Salmonella Oranienburg in onions from Chihuahua Mexico.
Distribution
Nationwide, NE, TN, TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-21
Company
Syracuse, UT
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Onions 52 has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Onions 52) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Onions 52 have FDA actions?
Onions 52 has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0230-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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