Harry & David WILD 'N SPICY
Reason Undeclared Wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese premix for the recalling firm.
Harry & David WILD 'N SPICY recall
Recalled by Fischer & Wieser Specialty Foods · Fredericksburg, TX, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared Wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese pre-mix for the recalling firm.
Undeclared allergens: Milk 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
Harry & David; WILD 'N SPICY; DOS QUESOS DIP; NET WT 1 lb.; (453g);Mild; in glass jars; MADE FOR HARRY AND DAVID, MEDFORD OR, HARRYANDDAVID.COM; 800-547-3033
Quantity: 2712 units (units are glass jars; cases contain 12 jars each for a total of 226 cases shipped.)
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 codes 10204
Where it was sold
Ohio Oregon
FDA's distribution note: OH, OR
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 milk, 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
- Fischer & Wieser Specialty Foods
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 19, 2014
- In FDA report of
- Jun 18, 2014
- Terminated
- Feb 4, 2015
- FDA recall number
- F-1411-2014 · event 67644
- 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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