Summary
The FDA issued a Class I for Mushroom Stir Fry Blend 9oz container sold individually by Taylor Farms Tennessee, Inc.. Reason: Positive Listeria monocytogenes in random sampling..
Details
Source
Food Recall
External ID
F-0122-2022
Action Date
2021-11-17
Status
Terminated
Category
food
Product Description
Mushroom Stir Fry Blend 9oz container sold individually
Lot/Code Info: Batch Number TFT289 Lot Number 30223112327 Product Number 61487 Sell By 10/22/21
Quantity Affected: 314 units
Reason for Recall
Positive Listeria monocytogenes in random sampling.
Distribution
Distributed to Kroger Retail locations in the following states: AL, AR, GA, IL, IN, KY, MS, TN. Product is stored at Taylor Farms warehouse. Taylor Farms picks and pallets Kroger's orders, then a third party comes and delivers the product to the retail locations.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-23
Company
Smyrna, TN
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.
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 (Taylor Farms Tennessee, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Taylor Farms Tennessee, Inc. have FDA actions?
This is the only FDA action we have on record for Taylor Farms Tennessee, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0122-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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