Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg. per case) - UPC 60580600120-8. Green
Summary
The FDA issued a Class I for Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pk by POTANDON PRODUCE LLC. Reason: Potential to be contaminated with Salmonella Oranienburg..
Details
Source
Food Recall
External ID
F-0114-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg. per case) - UPC 60580600120-8. Green Giant Fresh whole YELLOW onions in 3 lbs. flexible mesh bags, (16/3 lb. pkg. per case) - UPC 60580600123-9. Green Giant Fresh whole YELLOW onions in 5 lbs. flexible mesh bags, (10/5 lb. pkg. per case) - UPC 60580600170-3.
Lot/Code Info: Lot number and Julian Date on 2 lb. bag tag of Whole Yellow Onions: 42481-2 RA189 42481-2 RA194 42544-4 RA194 42544-4 RA197 42576-3 RA203 42576-3 RA204 42576-3 RA208 42562-5 RA202 42562-5 RA203 Lot number and Julian Date on 3 lb. bag tag of Whole Yellow Onions: 42481-3 RA194 42481-3 RA197 42481-3 RA200 42562-5 RA202 Lot number and Julian Date on 5 lb. bag tag of Whole Yellow Onions: 42481-3 RA194 42481-3 RA195 42481-3 RA197 42481-3 RA200 42562-8 RA204
Quantity Affected: Total 54,608 lbs. or 602 cases (25/2 lb. pkg per case); 96 cases (16/3 lb. pkg per case); 398 cases (10/5 lb. pkg per case)
Reason for Recall
Potential to be contaminated with Salmonella Oranienburg.
Distribution
Distributed in ND and MN.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-22
Company
Idaho Falls, ID
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 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
POTANDON PRODUCE LLC has 5 FDA actions in our database, including 5 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 (POTANDON PRODUCE LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does POTANDON PRODUCE LLC have FDA actions?
POTANDON PRODUCE LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0114-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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