Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M, 8 bottles
Summary
The FDA issued a Class I for Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 0 by Tulkoff Food Products, Inc.. Reason: Tulkoff Food Products Inc., 2229 Van Deman Street, Baltimore MD 21224 has initiated a recall of Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squ.
Details
Source
Food Recall
External ID
F-0756-2021
Action Date
2021-07-07
Status
Terminated
Category
food
Product Description
Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M, 8 bottles per case, keep refrigerated
Lot/Code Info: item number 098001, lot number 09.18.2021M
Quantity Affected: 140 Cases
Reason for Recall
Tulkoff Food Products Inc., 2229 Van Deman Street, Baltimore MD 21224 has initiated a recall of Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M because of undeclared allergens (Soy, Wheat)
Distribution
The product was distributed domestically to the following States: NJ, PA and MD.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-04
Company
Baltimore, MD
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 17 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 (Tulkoff Food Products, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tulkoff Food Products, Inc. have FDA actions?
This is the only FDA action we have on record for Tulkoff Food Products, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0756-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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