Food Recall Check
Class II · Moderate risk Ongoing Initiated Apr 19, 2021 (5 years ago)

Bake n Show¿ Muffin Tray 4 Cavity Large recall

Recalled by Genpak · Charlotte, NC, United States

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

Why it was recalled

The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.

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

Bake n Show¿ Muffin Tray 4 Cavity Large, Bake n Show¿ Muffin Tray 4 Cavity Large Shallow & Bake n Show¿ Muffin Tray 6 Cavity

Quantity: 4 Cavity - 55304-8B - 890 cases; 4 Cavity Shallow - 55304S-8B - 2,520 cases & 6 Cavity - 55306-8B - 1,875 cases

Food: 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.

4 Cavity - 55304-8B 4 Cavity Shallow - 55304S-8B 6 Cavity - 55306-8B

Where it was sold

Alabama Arizona California Colorado Connecticut Florida Georgia Illinois Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri North Carolina New Jersey Ohio Oregon Pennsylvania Texas Utah Washington Wisconsin

FDA's distribution note: Product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IL, KY, LA, MA, MD, MI, MN, MO, NC, NJ, OH, OR, PA, TX, UT, WA & WI. Product was also shipped to Canada.

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.

Recalling firm
Genpak
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 19, 2021
In FDA report of
Jun 9, 2021
FDA recall number
F-0649-2021 · event 87806
Official record
FDA enforcement report search

Also recalled with it (4 more products)

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

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