Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 23, 2015 (12 years ago)

Twin Tree Gardens Premium Rubs "bunkhouse" Chicken Rub recall

Recalled by Haddon House Food Products Inc · Medford, NJ, United States

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

Why it was recalled

Haddon House Food Products, Inc. is recalling Twin Tree Gardens Chicken Rub because it may contain undeclared Peanut Allergen.

Undeclared allergen: Peanut

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

Twin Tree Gardens Premium Rubs "bunkhouse" Chicken Rub, Net Wt. 2.75 oz. (77g), Distributed by: Flavor Delight, Inc., Richburg, South Carolina, UPC 041278582362

Quantity: 58 cases (696 units)

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 #'s 081817CHSASV55SV and 081917CHSA55SV

Where it was sold

Delaware Florida Illinois Indiana Kentucky Louisiana Maryland Maine Mississippi New Jersey New York Ohio Pennsylvania Tennessee Virginia Vermont

FDA's distribution note: DE, FL, IL, IN, KY, LA, MD, ME, MS, NJ, NY, OH, PA, TN, VA and VT

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 peanut; 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
Haddon House Food Products Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 23, 2015
In FDA report of
Apr 22, 2015
Terminated
Apr 21, 2017
FDA recall number
F-1952-2015 · event 70728
Official record
FDA enforcement report search