Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 14, 2021 (5 years ago)

Panera Lobster Bisque recall

Recalled by Blount Fine Foods Corporation · Fall River, MA, United States

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

Why it was recalled

Lobster bisque contains undeclared noodle with egg ingredient.

Undeclared allergens: Egg Shellfish

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

Panera Lobster Bisque, 16 oz.

Quantity: 17,992 units (2,987 cases)

Food: Seafood & fish

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/Unit Numbers: 030821-11K. Expiration date(s) or Use by Date(s) or expected shelf life of product: USE BY:05/17/2021 UPC Codes: 077958690300

Where it was sold

California Colorado Georgia Illinois Indiana Kansas Massachusetts Maryland Michigan Missouri North Carolina Nebraska New Jersey Oklahoma Oregon Pennsylvania Texas Virginia Washington Wisconsin

FDA's distribution note: CA, CO, GA, IL, IN, KS, MA, MD, MI, MO, NC, NE, NJ, OK, OR, PA, TX, VA, WA, 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 egg, shellfish; 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
Blount Fine Foods Corporation
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 14, 2021
In FDA report of
May 19, 2021
Terminated
Jan 11, 2022
FDA recall number
F-0486-2021 · event 87725
Official record
FDA enforcement report search

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