Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 20, 2017 (9 years ago)

Medium Coated Jo-Jo Wedges / 00040 recall

Recalled by Penobscot McCrum LLC · Belfast, ME, United States

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

Medium Coated Jo-Jo Wedges / 00040 (5lb bags)

Quantity: 951 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.

Lot Codes: 170117102000040 170117103000040 170117106000040 170117109000040 170117110000040 170117111000040 170117201000040 170228101000040 170228105000040 170228106000040 170228107000040 170228108000040 170228110000040 170412206000040 170412207000040 170412208000040 170412210000040 170412213000040 170412214000040 170412216000040

Where it was sold

Alabama Arkansas California Colorado Florida Georgia Iowa Illinois Indiana Kentucky Louisiana Massachusetts Maine Michigan Minnesota Mississippi North Carolina New Jersey New York Ohio Pennsylvania South Carolina Tennessee Texas Virginia Wisconsin

FDA's distribution note: LA, PA, OH, IL, KY, IN, TN, TX, FL, SC, CO, CA, AR, NC, MN, ME, AL, MI, VA, NY, IA, NJ, MA, MS, GA, WI

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
Penobscot McCrum LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 20, 2017
In FDA report of
Aug 30, 2017
Terminated
Nov 3, 2017
FDA recall number
F-3225-2017 · event 77477
Official record
FDA enforcement report search

Also recalled with it (9 more products)

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