Super Twa Mushroom Mixed Mushrooms; New Wt/When Packed) 14.11 oz. (400g) Keep refrigerated. UPC: 6957937481850
Summary
The FDA issued a Class I for Super Twa Mushroom Mixed Mushrooms; New Wt/When Packed) 14.11 oz. (400g) Keep by Farm Fresh Produce LLC. Reason: California Department of Public Health of Public Health sampled product and found it to contain Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1008-2022
Action Date
2022-04-27
Status
Terminated
Category
food
Product Description
Super Twa Mushroom Mixed Mushrooms; New Wt/When Packed) 14.11 oz. (400g) Keep refrigerated. UPC: 6957937481850
Lot/Code Info: No codes on packages
Quantity Affected: 160 cases
Reason for Recall
California Department of Public Health of Public Health sampled product and found it to contain Listeria monocytogenes.
Distribution
CA Only
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-22
Company
Vernon, CA
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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Farm Fresh 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 Farm Fresh Produce LLC have FDA actions?
This is the only FDA action we have on record for Farm Fresh Produce LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1008-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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