Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 20, 2017 (10 years ago)

Kwei Chow brand Prime Spicy Pot Paste recall

Recalled by Kwei Chow Sauce Industry Co., Ltd. · New Taipei City, N/A, Taiwan

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Products contain undeclared wheat.

Undeclared allergen: 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

Kwei Chow brand Prime Spicy Pot Paste, net weight 7.10 Oz, sauce in glass jars, shelf stable

Quantity: 1680 jars

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.

Manufacturing dates 2016.10.20, 2016.01.28, 2017.01.10, 2016.12.12. Ship dates 2016.12.19, 2016.02.26, 2017.01.12. Expiry dates 2018.10.19, 2018.01.27, 2019.01.09, 2018.12.11. Codes SA1612, SA1601, JAN092019, DEC112018

Where it was sold

FDA's distribution note: Product was distributed to at least three distributors in the US.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to 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
Kwei Chow Sauce Industry Co., Ltd.
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 20, 2017
In FDA report of
Apr 12, 2017
Terminated
May 22, 2017
FDA recall number
F-1835-2017 · event 76812
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.