Tulkoff Spicy Kimchi Aioli recall
Recalled by Tulkoff Food Products, Inc. · Baltimore, MD, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
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)
Undeclared allergens: Soy Wheat
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Quantity: 140 Cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
item number 098001, lot number 09.18.2021M
Where it was sold
Maryland New Jersey Pennsylvania
FDA's distribution note: The product was distributed domestically to the following States: NJ, PA and MD.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Tulkoff Food Products, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 4, 2021
- In FDA report of
- Jul 7, 2021
- Terminated
- Oct 7, 2021
- FDA recall number
- F-0756-2021 · event 88062
- Official record
- FDA enforcement report search