Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 31, 2014 (13 years ago)

Hudson Valley Homestead Bushwhacker's Savory Sauce recall

Recalled by Charlemagnes Tree Farm Ltd · Craryville, NY, United States

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

Why it was recalled

Charlemagne's Tree Farm, Ltd. dba HUDSON VALLEY HOMESTEAD recalled BUSHWHACKER'S Savory Sauce Mild and Hot & Spicy due to Undeclared Anchovies.

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

HUDSON VALLEY HOMESTEAD BUSHWHACKER'S SAVORY SAUCE, Mild, Net Wt. 14 oz., UPC: 7 51122 00091 0, Hudson Valley Homstead 102 Sheldon Lane Craryville, New York 12521 (518) 851-7336, www.hudsonvalleyhomstead.com

Quantity: 2100 bottles

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.

all lots

Where it was sold

Massachusetts Maine New York

FDA's distribution note: NY, ME, MA

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
Charlemagnes Tree Farm Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 31, 2014
In FDA report of
Mar 19, 2014
Terminated
Jun 1, 2018
FDA recall number
F-1650-2014 · event 67365
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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

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