Green Giant Fresh brand, Whole YELLOW Onions packaged in 2 lb. flexible mesh bags, UPC 60580600120-8. Green Giant Fresh
Summary
The FDA issued a Class I for Green Giant Fresh brand, Whole YELLOW Onions packaged in 2 lb. flexible mesh bag by POTANDON PRODUCE LLC. Reason: Salmonella Oranienburg. Products are supplied by Keeler Family Farm..
Details
Source
Food Recall
External ID
F-0183-2022
Action Date
2021-11-24
Status
Terminated
Category
food
Product Description
Green Giant Fresh brand, Whole YELLOW Onions packaged in 2 lb. flexible mesh bags, UPC 60580600120-8. Green Giant Fresh brand, Whole YELLOW Onions packaged in 3 lb. flexible mesh bags, UPC 60580600123-9. Green Giant Fresh brand, Whole YELLOW Onions packaged in 5 lb. flexible mesh bags, UPC 60580600170-3.
Lot/Code Info: Lot # and Julian Date on bag tag of whole YELLOW onions in 2 lbs. bag: 42543-2 RA201 42600-3 RA208 42600-3 RA209 42542-2 RA201 42542-5 RA197 42542-5 RA202 Lot # and Julian Date on bag tag of whole YELLOW onions in 3 lbs. bag: 42543-2 RA201 42543-2 RA203 42543-2 RA204 42542-5 RA202 Lot # and Julian Date on bag tag of whole YELLOW onions in 5 lbs. bag: 42543-2 RA200 42543-2 RA201 42543-2 RA202 42543-2 RA203 42543-2 RA204 42542-2 RA203 ADDITIONAL LOTS: 049008, 119008, and 149007.
Quantity Affected: Total 61,206 lbs or 359 cases (25/2 lb. pkg per case); 397 cases (16/3 lb. pkg per case); 484 cases (10/5 lb. pkg per case);
Reason for Recall
Salmonella Oranienburg. Products are supplied by Keeler Family Farm.
Distribution
distributed in MN and ND.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-25
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 88 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-0183-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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