Food Recall Check
Class I · High risk Terminated Initiated Mar 13, 2022 (5 years ago)

Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties recall

Recalled by Cavendish Farms · Dieppe, N/A, Canada

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

Why it was recalled

Undeclared barley and wheat flour

Undeclared allergen: 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

Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties Net Wt, 42.3 (1.2 kg). 12 retail packages per case, 20 patties per retail tray pack. UPC: 0 56210 34217 1

Quantity: 441 cases

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.

BEST BEFORE 2024 FE 01

Where it was sold

Connecticut Delaware Massachusetts Maryland New Hampshire New Jersey New York Pennsylvania Rhode Island

FDA's distribution note: Product was distributed to 2 warehouse locations in PA. Further distributed to retail stores in CT, DE, MD, MA, NH, NJ, NY, PA, and RI.

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 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
Cavendish Farms
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 13, 2022
In FDA report of
Apr 6, 2022
Terminated
Aug 5, 2022
FDA recall number
F-0959-2022 · event 89796
Official record
FDA enforcement report search