R. Walters Foods, Limited Liability Corporation Recall: Product contains undeclared hydrolyzed soy protein.

🇺🇸 United States

1. October 29, 2024 - Recall initiated
2. December 4, 2024 - Reported by source
3. March 3, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0147-2025

Event ID

95657

Status

Terminated

Classification

Class II

Company

R. Walters Foods, Limited Liability Corporation

Product description

Hannaford brand seafood salad; Net Wt. 12 oz. (340g); INGREDIENTS: SEAFOOD BLEND (FISH PROTEIN [ALASKA POLLOCK AND/OR PACIFIC WHITING], WATER, WHEAT STARCH, SUGAR, SORBITOL, MODIFIED POTATO STARCH, CONTAINS 2% OR LESS OF: NATURAL AND ARTIFICIAL CRAB FLAVORS [SWIMMING CRAB, SNOW CRAB], MIRIN WINE [SAKE, SUGAR, SALT, WATER, YEAST EXTRACT], EGG WHITES, SALT, SOYBEAN OIL, SODIUM TRIPOLYPHOSPHATE, TETRASODIUM PYROPHOSPHATE, CARMINE, PAPRIKA OLEORESIN, COLOR ADDED), MAYONNAISE (SOYBEAN OIL, EGG YOLK, VINEGAR, WATER, SUGAR, SALT, SPICES, NATURAL FLAVOR), CELERY, WATER, NATURAL FLAVORS, MODIFIED FOOD STARCH, NISIN, CITRIC ACID.; CONTAINS: EGGS, WHEAT, ALASKA POLLOCK, PACIFIC WHITING, SWIMMING CRAB, SNOW CRAB; DISTRIBUTED BY: HANNAFORD BROS. CO., LLC; UPC: 0 41268 25161 2

Quantity

278 cases

Reason

Product contains undeclared hydrolyzed soy protein.

Recall initiation date

October 29, 2024

Report date

December 4, 2024

Classification date

Not published in this source record

Termination date

March 3, 2025

Distribution pattern

Maine, New Hampshire, Vermont, Massachusetts, New York.

UPC, lot, and code information

USE By : 11/13/24 and USE By : 11/14/24

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: R. Walters Foods, Limited Liability Corporation

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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