Hood Everything Bagel Cottage Cheese recall

Recalled by HP Hood LLC · Lynnfield, MA, United States

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

Why it was recalled

Product may contain foreign objects (plastic).

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Hood Everything Bagel Cottage Cheese, 16 oz

Quantity: 391,824 cases (total)

Food: Cheese Bread & bakery

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.

Products being recalled have a best by date between Oct 24 2022 through Dec 12 2022

Where it was sold

Alabama Arizona California Colorado Connecticut Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Rhode Island Texas Utah Virginia Vermont Washington Wisconsin Wyoming

FDA's distribution note: Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Mexico, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, Texas, Utah, Vermont, Virginia, Washington, Wisconsin, Wyoming

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: HP Hood LLC
Initiated by: Voluntary: Firm initiated
Recall initiated: Oct 25, 2022
In FDA report of: Nov 9, 2022
Terminated: Mar 1, 2023
FDA recall number: F-0127-2023 · event 91053
Official record: FDA enforcement report search

Also recalled with it (12 more products)

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

Class II · Moderate risk Terminated Foreign material Oct 25, 2022