Hudson Valley Homestead Bushwhacker's Savory Sauce
Reason Charlemagne's Tree Farm, Ltd. dba HUDSON VALLEY HOMESTEAD recalled BUSHWHACKER'S Savory Sauce Mild and Hot & Spicy due to Undeclared Anchovies.
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, Hot & Spicy, Net Wt. 14 oz., UPC 7 51122 00092 1, 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-1651-2014 · 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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