Food Recall Check
Class I · High risk Terminated Initiated Feb 5, 2021 (6 years ago)

Spicy Red Curry Sauce recall

Recalled by Barbara's Orchard/Delicae Gourmet · Tarpon Springs, FL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared allergen: Shrimp

Undeclared allergen: Shellfish

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

Spicy Red Curry Sauce, 12 fl. oz. (355ml), UPC code #643558406810

Quantity: 52 cases / 12 per case

Food: Sauces, dips & dressings

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.

Batch No. 20084; best by date: 5-28-23 Batch No. 19404; best by date: 9-10-22 Batch No. 19158; best by date: 4-25-22 Batch No. 18213; best by date: 11-19-21

Where it was sold

Colorado Florida Illinois Missouri New York Pennsylvania Virginia Wyoming

FDA's distribution note: U.S distribution to the following: Springfield, MO; Crystal Lake, IL; Palisade, CO; Colorado Springs, CO; Long Lake, NY; Long Grove, IL; Sheridan, WY; Venice, FL; Pittsburgh, PA; Nassawadox, VA.

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 shellfish; 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
Barbara's Orchard/Delicae Gourmet
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 5, 2021
In FDA report of
Mar 3, 2021
Terminated
Jul 20, 2021
FDA recall number
F-0321-2021 · event 87287
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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