E-Z Spuds Inc. fresh cut onion products (10, 20, 30 lbs) diced, sliced, Julienne, whole peeled
Summary
The FDA issued a Class I for E-Z Spuds Inc. fresh cut onion products (10, 20, 30 lbs) diced, sliced, Julienne by E-Z Spuds Inc. Reason: Potential contamination with Salmonella.
Details
Source
Food Recall
External ID
F-0123-2022
Action Date
2021-11-17
Status
Terminated
Category
food
Product Description
E-Z Spuds Inc. fresh cut onion products (10, 20, 30 lbs) diced, sliced, Julienne, whole peeled
Lot/Code Info: Mfg Date: JUL 14, '21 JUL 15, '21 JUL 16, '21 JUL 19, '21 JUL 20, '21 JUL 21, '21 JUL 22, '21 JUL 23, '21 JUL 26, '21 JUL 27, '21 JUL 28, '21 JUL 29, '21 JUL 30, '21 AUG 02, '21 AUG 03, '21 AUG 04, '21 AUG 05, '21 AUG 06, '21 AUG 09, '21 AUG 10, '21 AUG 11, '21 AUG 12, '21 AUG 13, '21 AUG 16, '21 AUG 17, '21 AUG 19, '21 AUG 20, '21 AUG 23, '21 AUG 24, '21 AUG 25, '21 AUG 26, '21 AUG 27, '21 AUG 30, '21 AUG 31, '21 SEP 01, '21 SEP 02, '21 SEP 03, '21 SEP 07, '21 SEP 08, '21 SEP 09, '21
Quantity Affected: 5,630 cases
Reason for Recall
Potential contamination with Salmonella
Distribution
Manufacturers and Food service establishments in the Chicago, IL metro area
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-21
Company
Melrose Park, IL
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 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
E-Z Spuds Inc has 11 FDA actions in our database, including 11 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 (E-Z Spuds Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does E-Z Spuds Inc have FDA actions?
E-Z Spuds Inc has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0123-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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