Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 7, 2017 (9 years ago)

Small White Button Mushroom Regular Batter recall

Recalled by Oxford Frozen Foods Plant 1 · Oxford Station, Nova Scotia, Canada

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

Why it was recalled

Product may contain undeclared milk.

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

Small White Button Mushroom Regular Batter: ATLANTIC GOLD Battered Mushrooms Net Weight 5 lb (2.27 kg) - 34086; Atlantic Gold Battered Mushrooms 6 x 2 lbs 12 lbs - 34112;

Quantity: 36,983 cases (total for all products)

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.

Jan 11/17 to Jun 6/17 YYMMDD 170111 to 170606

Where it was sold

Connecticut Massachusetts Maine North Carolina New Hampshire New Jersey New York Pennsylvania Rhode Island Virginia Wisconsin

FDA's distribution note: RI, ME, NY, CT, PA, VA, NJ, MA, NC, WI, NH

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 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
Oxford Frozen Foods Plant 1
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 7, 2017
In FDA report of
Jul 12, 2017
Terminated
Oct 28, 2019
FDA recall number
F-2446-2017 · event 77483
Official record
FDA enforcement report search

Also recalled with it (5 more products)

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