Food Recall Check
Class I · High risk Terminated Initiated Aug 20, 2013 (13 years ago)

Hartley's Potato Chips Salt & Vinegar recall

Recalled by Hartleys Potato Chip Company Inc · Lewistown, PA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared lactose (milk) in seasoning sub-ingredient used in the manufacturing of Hartley's Salt & Vinegar Potato Chips.

Undeclared allergen: Milk

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

Hartley's Potato Chips Salt & Vinegar 4.5 oz and 2.5 oz bags Hartley's Potato Chip Co., Inc, Lewistown, PA Ingredients: potatoes, vegetable shortening, salt, lactose, sodium diacetate, salt, malic acid, sodium citrate, with not more than 2% silicon dioxide and partially hydrogenated soybean and/or cottonseed oil.

Quantity: 4549 bags; 722 lb.

Food: Chips & snacks

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: Oct 7 2013 and Oct 30 2013

Where it was sold

Pennsylvania

FDA's distribution note: Pennsylvania only.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; 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
Hartleys Potato Chip Company Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 20, 2013
In FDA report of
Oct 23, 2013
Terminated
Aug 27, 2014
FDA recall number
F-0001-2014 · event 66053
Official record
FDA enforcement report search

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