Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 22, 2017 (10 years ago)

Kangaroo jerky brand Trophy Series recall

Recalled by Whiskey Hill Smokehouse · Hubbard, OR, United States

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

Why it was recalled

kangaroo jerky is recalled due to undeclared soy lecithin.

Undeclared allergen: Soy

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

Kangaroo jerky, brand Trophy Series, heat treated shelf stable packaged in hermetically sealed packages. Net wt. 3 oz. UPC 16831 00550

Quantity: 465 lbs.

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.

Sell By Dates: JULY 4, 2017 SEPT 12, 2017 FEB 9, 2018 Lot Numbers: 183163 254163 28172

Where it was sold

California Florida Illinois Massachusetts North Carolina New York Oregon Pennsylvania Texas Washington

FDA's distribution note: CA, FL, IL, MA, NC, NY, OR, OR, PA, TX, and WA.

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 soy; 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
Whiskey Hill Smokehouse
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 22, 2017
In FDA report of
Apr 26, 2017
Terminated
Jul 5, 2017
FDA recall number
F-1964-2017 · event 76936
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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