Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 24, 2014 (12 years ago)

Ava's Berry Nutty Mix trail mix packed in recall

Recalled by Northhampton Peanut Company · Severn, NC, United States

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

Why it was recalled

Undeclared Allergen: Sulfites

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

Ava's Berry Nutty Mix trail mix packed in 20 oz. clear plastic containers.

Quantity: unknown

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.

UPC Code: 8 10111 01088 7 (9 oz) and UPC Code: 8-10111-01116-7 (20 oz), Lot numbers: 4214, 4914, 5614, 5814, 6614, 7214, 7614, 8614, 8814, 9014, 9814, 10014, 10814, 10914, 11414, 12114, 13914, 14014, 15414, 15714, 16414, 17514, 17614, 19114, 19514, 19714, 20514, 20914, 21914, 22414, 24514, 24614, 25814, 26314, 26514, 27014, 28814, 29414, 29514, 30714, 31514, 32214 and 32914.

Where it was sold

Connecticut Massachusetts New Jersey New York Pennsylvania

FDA's distribution note: CT, MA, NJ, NY and PA.

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. 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
Northhampton Peanut Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 24, 2014
In FDA report of
Jun 10, 2015
Terminated
Oct 7, 2016
FDA recall number
F-2403-2015 · event 70195
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.