Pico De Gallo
Reason Potential contamination with Salmonella.
FAIRWAY brand CONDIMENT GRILLING SAUCE recall
Recalled by Wolfgang B. Gourmet Foods, Inc. · Catskill, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The Grilling Sauce contains undeclared fish (anchovies), a a sub-ingredient in the Worcestershire Sauce ingredient used in making the product.
Undeclared allergen: Fish
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
FAIRWAY brand CONDIMENT GRILLING SAUCE, NET WT 12 oz (340 g), UPC 7 58940 70609 3 -- Distributed By: Fairway Group Central Services LLC New York, New York 10027 --- The product is packaged in a glass bottle, 12 bottles per case.
Quantity: 348 units
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.
Lot 340 GRSC with a "use by" date of 03/08/2014, and Lot 357 GRSC with a "use by" date 03/25/2014 (located on side of glass bottle)
Where it was sold
Connecticut New Jersey New York
FDA's distribution note: NY, NJ, and CT
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 fish; 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
- Wolfgang B. Gourmet Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 20, 2014
- In FDA report of
- Apr 2, 2014
- Terminated
- Apr 1, 2015
- FDA recall number
- F-1684-2014 · event 67600
- Official record
- FDA enforcement report search
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